Noninvasive Prenatal Diagnosis of Congenital Adrenal Hyperplasia Using Cell-Free Fetal DNA in Maternal Plasma-Reference-Cited by-同舟云学术

Noninvasive Prenatal Diagnosis of Congenital Adrenal Hyperplasia Using Cell-Free Fetal DNA in Maternal Plasma

Published:2014-06-01 Issue:6 Volume:99 Page:E1022-E1030
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

New Maria I.¹,Tong Yu K.²³,Yuen Tony¹,Jiang Peiyong²³,Pina Christian¹,Chan K. C. Allen²³,Khattab Ahmed¹,Liao Gary J. W.²³,Yau Mabel¹,Kim Se-Min¹,Chiu Rossa W. K.²³,Sun Li¹,Zaidi Mone¹,Lo Y. M.²³

Affiliation:

1. Departments of Pediatrics and Medicine (M.I.N., T.Y., C.P., A.K., M.Y., S.-M.K., L.S., M.Z.), Mt Sinai School of Medicine, New York, New York 10029

2. Centre for Research into Circulating Fetal Nucleic Acids (Y.K.T., P.J., K.C.A.C., G.J.W.L., R.W.K.C., Y.M.L.), Li Ka Shing Institute of Health Sciences, Hong Kong

3. Department of Chemical Pathology (Y.K.T., P.J., K.C.A.C., G.J.W.L., R.W.K.C., Y.M.L.), The Chinese University of Hong Kong, Hong Kong SAR, China

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/99/6/E1022/9045103/jcem1022.pdf

Reference23 articles.

1. Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Pang;Pediatrics,1988

2. Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency;New;Proc Natl Acad Sci USA,2013

3. Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency;New,2014

4. Structure-phenotype correlations of human CYP21A2 mutations in congenital adrenal hyperplasia;Haider;Proc Natl Acad Sci USA,2013