(Q44587834)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

title

Birth prevalence of disorders detectable through newborn screening by race/ethnicity (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

author name string

Lisa Feuchtbaum

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Jennifer Carter

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Sunaina Dowray

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

Fred Lorey

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

language of work or name

English

0 references

publication date

5 July 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

volume

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

page(s)

937-945

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22766612%20AND%20SRC:MED&resulttype=core&format=json

Newborn screening: toward a uniform screening panel and system

7 February 2020

cites work

1 reference

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Universal newborn screening for Hb H disease in California

21 January 2018

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Maple syrup urine disease: identification and carrier-frequency determination of a novel founder mutation in the Ashkenazi Jewish population

21 January 2018

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Prospective diagnosis of 2-methylbutyryl-CoA dehydrogenase deficiency in the Hmong population by newborn screening using tandem mass spectrometry.

21 January 2018

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A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK.

21 January 2018

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Newborn screening for hemoglobinopathies in California

21 January 2018

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Trends in incidence rates of congenital hypothyroidism related to select demographic factors: data from the United States, California, Massachusetts, New York, and Texas

21 January 2018

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Molecular genetic confirmatory testing from newborn screening samples for the common African-American, Asian Indian, Southeast Asian, and Chinese beta-thalassemia mutations

21 January 2018

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Demographics of the UK cystic fibrosis population: implications for neonatal screening

21 January 2018

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Newborn screening for non-sickling hemoglobinopathies

21 January 2018

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Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening

21 January 2018

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The context and approach for the California newborn screening short- and long-term follow-up data system: preliminary findings

21 January 2018

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Asian immigration and public health in California: thalassemia in newborns in California

21 January 2018

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Clinical outcomes in infants with cystic fibrosis transmembrane conductance regulator (CFTR) related metabolic syndrome

21 January 2018

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

21 January 2018

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Diagnostic re-evaluation of children with congenital hypothyroidism

21 January 2018

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Time trend and geographic distribution of treated patients with congenital hypothyroidism relative to the number of available endocrinologists in Japan.

21 January 2018

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Diagnoses of newborns and mothers with carnitine uptake defects through newborn screening

21 January 2018

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Nationwide survey of extended newborn screening by tandem mass spectrometry in Taiwan

21 January 2018

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High prevalence of short-chain acyl-CoA dehydrogenase deficiency in the Netherlands, but no association with epilepsy of unknown origin in childhood.

21 January 2018

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Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders

21 January 2018

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Ethnicity, ancestry, and race in molecular epidemiologic research

21 January 2018

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The importance of race and ethnic background in biomedical research and clinical practice

21 January 2018

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Genes, race, and population: avoiding a collision of categories.

21 January 2018

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Health status and healthcare use in a national sample of children with sickle cell disease

21 January 2018

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Mutation distribution in expanded screening for cystic fibrosis: making up the balance in a context of ethnic diversity

21 January 2018

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7 January 2021

Alpha-thalassemia (3.7 kb deletion) in a population from the Brazilian Amazon region: Santarém, Pará State.

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7 January 2021

Risk factors for congenital hypothyroidism: An investigation of infant's birth weight, ethnicity, and gender in California, 1990-1998

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7 January 2021

Survey of neonatal screening for primary hypothyroidism in England, Wales, and Northern Ireland 1982-4.

1 reference

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7 January 2021

Population estimates of sickle cell disease in the U.S.

1 reference

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7 January 2021