(Q35193941)

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Genetic screening

scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

7 August 2017

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Europe PubMed Central

Genetic screening. (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

1

object named as

Wylie Burke

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

author name string

Beth Tarini

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Nancy A Press

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

James P Evans

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

publication date

27 June 2011

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Epidemiologic Reviews

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

33

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

148-164

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Carrier testing for severe childhood recessive diseases by next-generation sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Patients-in-waiting: Living between sickness and health in the genomics era.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Relationships among health-related quality of life, pulmonary health, and newborn screening for cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

A three-step workflow procedure for the interpretation of array-based comparative genome hybridization results in patients with idiopathic mental retardation and congenital anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Weighing the evidence for newborn screening for early-infantile Krabbe disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Congenital hypothyroidism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Genomic medicine--an updated primer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Clinical assessment incorporating a personal genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Epidemiologic and genetic aspects of spina bifida and other neural tube defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

An evidence development process for newborn screening

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Family history in public health practice: a genomic tool for disease prevention and health promotion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Newborn screening: an appeal for improved parent education

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

ACOG Committee Opinion No. 442: Preconception and prenatal carrier screening for genetic diseases in individuals of Eastern European Jewish descent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Consent for newborn screening: the attitudes of health care providers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Massively parallel sequencing: the next big thing in genetic medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Impact of false-positive newborn metabolic screening results on early health care utilization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

The 50th anniversary of the discovery of trisomy 21: the past, present, and future of research and treatment of Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Clinical practice. Prenatal screening for aneuploidy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Impact of a new national screening policy for Down's syndrome in Denmark: population based cohort study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Newborn screening of metabolic disorders: recent progress and future developments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

The consequences of extended newborn screening programmes: do we know who needs treatment?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Medical legal issues in prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

From new screens to discovered genes: the successful past and promising present of single gene disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

ACOG Practice Bulletin No. 78: hemoglobinopathies in pregnancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Universal newborn screening and adverse medical outcomes: a historical note

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Potential impact of newborn screening for cystic fibrosis on child survival: a systematic review and analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Newborn screening may fail to identify intermediate forms of maple syrup urine disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

A vision of the future of newborn screening

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Newborn screening technology: proceed with caution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

The epidemiology of medium chain acyl-CoA dehydrogenase deficiency: an update.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

From public health emergency to public health service: the implications of evolving criteria for newborn screening panels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

ACOG Committee Opinion. Number 325, December 2005. Update on carrier screening for cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

The survival advantage of patients with cystic fibrosis diagnosed through neonatal screening: evidence from the United States Cystic Fibrosis Foundation registry data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility: recommendation statement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

From genetics to genomics: using gene-based medicine to prevent disease and promote health in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Psychosocial risk associated with newborn screening for cystic fibrosis: parents' experience while awaiting the sweat-test appointment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Newborn screening for cystic fibrosis: evaluation of benefits and risks and recommendations for state newborn screening programs.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Prenatal diagnosis, pregnancy terminations and prevalence of Down syndrome in Atlanta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Socioeconomic and state-level differences in prenatal diagnosis and live birth prevalence of Down's syndrome in the United States.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

A practical approach to risk assessment to prevent coronary artery disease and its complications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Disability rights critique of prenatal genetic testing: Reflections and recommendations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Population screening in the age of genomic medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Standards and guidelines for CFTR mutation testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Screening for thalassemia: a model of success.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Cost-effectiveness of microsatellite instability screening as a method for detecting hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

The Dor Yeshorim story: community-based carrier screening for Tay-Sachs disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

National Institutes of Health Consensus Development Conference Statement: phenylketonuria: screening and management, October 16-18, 2000.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Estimating the efficacy and efficiency of cascade genetic screening

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Rare diseases and the assessment of intervention: what sorts of clinical trials can we use?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

US newborn screening system guidelines II: follow-up of children, diagnosis, management, and evaluation. Statement of the Council of Regional Networks for Genetic Services (CORN).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Neonatal screening for sickle cell disorders: what about the carrier infants?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Tay-sachs disease. Detection of heterozygotes and homozygotes by serum hexosaminidase assay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Neonatal screening and genetic counseling for sickle cell trait

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Fatal knowledge? Prenatal diagnosis and sex selection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Conceiving a fetus for bone marrow donation: an ethical problem in prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Is a genetic screening test ready when the lawyers say it is?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Prenatal screening for hemoglobinopathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Prenatal Genetic Diagnosis in 3000 Amniocenteses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

13 July 2018

Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Gradual implementation of first trimester screening in a population with a prior screening strategy: population based cohort study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Maple syrup urine disease: further evidence that newborn screening may fail to identify variant forms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Association between carrier screening and incidence of cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

ACOG committee opinion No. 432: spinal muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Newborn screening showing decreasing incidence of cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Patient advocacy in newborn screening: continuities and discontinuities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Prenatal screening, autonomy and reasons: the relationship between the law of abortion and wrongful birth.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Newborn screening for developmental disabilities: reframing presumptive benefit.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Effect of a phenylalanine-restricted diet on patients with phenylketonuria; clinical observations in three cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Impact of public health strategies on the birth prevalence of cystic fibrosis in Brittany, France

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Phenylketonuria in adulthood: a collaborative study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Genetic screening programs and public policy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Mandatory versus voluntary consent for newborn screening?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

27 September 2018

Questioning the consensus: managing carrier status results generated by newborn screening

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

15 November 2018

Ethics, evidence, and cost in newborn screening

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166195

15 November 2018

Preparing for a consumer-driven genomic age

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

American Gastroenterological Association medical position statement: hereditary colorectal cancer and genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Birth prevalence of Down syndrome in Singapore from 1993 to 1998

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

State newborn screening in the tandem mass spectrometry era: more tests, more false-positive results

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impact of prenatal diagnosis on the prevalence of live births with Down syndrome in the eastern half of Switzerland 1980-1996

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of phenylalanine intake on phenylketonuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The tandem mass spectrometry newborn screening experience in North Carolina: 1997-2005

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Birth prevalence and survival in cystic fibrosis: a national cohort study in the Netherlands

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The impact of maternal serum screening on the birth prevalence of Down's syndrome and the use of amniocentesis and chorionic villus sampling in South Australia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Making the case for objective performance metrics in newborn screening by tandem mass spectrometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic Fibrosis Foundation practice guidelines for the management of infants with cystic fibrosis transmembrane conductance regulator-related metabolic syndrome during the first two years of life and beyond.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cystic fibrosis birth rates in Canada: a decreasing trend since the onset of genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expanded newborn screening for biochemical disorders: the effect of a false-positive result

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic testing for cystic fibrosis. National Institutes of Health Consensus Development Conference Statement on genetic testing for cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An association between low maternal serum α-fetoprotein and fetal chromosomal abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Newborn screening--setting evidence-based policy for protection

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenylketonuria variants in Ontario

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevention of thalassaemia in Cyprus

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prophylaxis with oral penicillin in children with sickle cell anemia. A randomized trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recommendations for effective newborn screening communication: results of focus groups with parents, providers, and experts

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of anencephaly through maternal serum-alphafetoprotein measurement

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tay-Sachs disease: heterozygote screening and prenatal diagnosis--U.S. experience and world perspective

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic Counseling: Clinical Geneticists' Views

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Current controversies in prenatal diagnosis 3: For prenatal diagnosis, should we offer less or more than metaphase karyotyping?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lights! Camera! Action!

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ACOG Practice Bulletin No. 88, December 2007. Invasive prenatal testing for aneuploidy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Practice patterns of obstetrician-gynecologists regarding preconception and prenatal screening for cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Declining prevalence of cystic fibrosis since the introduction of newborn screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prevalence of live birth Down syndrome in the region of Primorsko-goranska County in Croatia, 1996-2005: the impact of screening and amniocentesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of amniocentesis in the intrauterine detection of genetic disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

False negative 17-hydroxyprogesterone screening in children with classical congenital adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consensus conference. Newborn screening for sickle cell disease and other hemoglobinopathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic counseling

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal PKU Collaborative Study: pregnancy outcome and postnatal head growth

1 reference

https://pubmed.ncbi.nlm.nih.gov/21709145

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/EPIREV/MXR008

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

ResearchGate publication ID

0 references

Sitelinks

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