Statement of the American College of Medical Genetics on Universal Newborn Hearing Screening-Reference-Cited by-同舟云学术

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Statement of the American College of Medical Genetics on Universal Newborn Hearing Screening

Published:2000-03 Issue:2 Volume:2 Page:149-150
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Nance Walter E.,Cunningham George C.,Davis Jessica G.,Morton Cynthia C.,Elsas Louis J.,Finitzo Teresa,Falk Rena E.,Ing Paul S.,Pandya Arti,McCabe Edward R.B.,Smith Richard J.H.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference15 articles.

1. A NEW GENETIC ABNORMALITY RESULTING IN GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DEFICIENCY

2. Newborn screening for galactosemia and other galactose metabolic defects

3. Long-term prognosis in galactosaemia: Results of a survey of 350 cases

4. Growth and development of children with galactosemia

5. Long-term Follow-up of Galactosaemia

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. “My Plate is Full”: Reasons for Declining a Genetic Evaluation of Hearing Loss;Journal of Genetic Counseling;2017-10-04

2. Hearing Impairment;Health Care for People with Intellectual and Developmental Disabilities across the Lifespan;2016

3. New Directions in Cytogenetic and Molecular Testing of the Neonate;Seminars in Perinatology;2005-06

4. Audiometric evaluation of carriers of the connexin 26 mutation 35delG;European Archives of Oto-Rhino-Laryngology;2005-05-14

5. Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness;Clinical Genetics;2004-06-08

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