(Q36599826)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

review article

1 reference

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

0 references

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

author name string

L Laird

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

E N Anionwu

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

language of work or name

English

0 references

publication date

1 August 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

volume

313

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

issue

7054

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

page(s)

407-411

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

The genetic testing of children. Working Party of the Clinical Genetics Society (UK)

18 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

GIG response to the UK Clinical Genetics Society report "The genetic testing of children"

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Effects of genetic counseling on parental self-concepts

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

The Health Orientation Scale: a measure of feelings about sickle cell trait

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Prediction and diagnosis of sickling disorders in neonates

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Knowledge and perceptions of haemoglobinopathy carrier screening among general practitioners in Cardiff

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Duty to disclose in medical genetics: a legal perspective

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Non-paternity and prenatal genetic screening

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Discrimination as a consequence of genetic testing

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Genetic testing for familial hypertrophic cardiomyopathy in newborn infants. A positive screening test for an untreatable condition provides psychological relief from uncertainty

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Sickle cell "nondisease". A potentially serious public health problem

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Neonatal screening and genetic counseling for sickle cell trait

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Evaluation of eight and a half years of neonatal screening for haemoglobinopathies in Birmingham

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Neonatal screening for sickle cell diseases in Camberwell: results and recommendations of a two year pilot study

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Newborn screening for sickle cell disease and other hemoglobinopathies. Northern California's experience.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Neonatal screening for sickle cell disease in a metropolitan university hospital: efficacy and problems

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Mothers' consent to screening newborn babies for disease

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

Universal screening for hemoglobinopathies using high-performance liquid chromatography: clinical results of 2.2 million screens.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2351830

A private view of heterozygosity: eight-year follow-up study on carriers of the Tay-Sachs gene detected by high school screening in Montreal

20 September 2018

1 reference

12 December 2020

DNA microextraction from dried blood spots on filter paper blotters: potential applications to newborn screening

1 reference

12 December 2020

Training and needs of health visitors in the haemoglobinopathies

1 reference

12 December 2020

Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screening

1 reference

12 December 2020

Parental receptivity to neonatal sickle trait identification

1 reference

12 December 2020

Newborn screening for hemoglobinopathies in Colorado. The first 10 years

1 reference

12 December 2020

Non-paternity and prenatal genetic screening

1 reference

12 December 2020

RNA analysis from newborn screening dried blood specimens

1 reference

12 December 2020

The stigma of disease: implications of genetic screening

1 reference

12 December 2020

Comparison of liquid and dried blood for neonatal hemoglobinopathy screening: laboratory and programmatic issues

1 reference

12 December 2020

Sickle cell and thalassaemia: some priorities for nursing research

1 reference

12 December 2020

Identifiers

DOI

10.1136/BMJ.313.7054.407

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8761233%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

PubMed publication ID

8761233

1 reference