Unknown syndrome: abnormal facies, hypothyroidism, and severe retardation: a second patient.
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Reference2 articles.
1. congcnitail hcirt defccts. hypothvroidism. aind sevcrc rctardation;J Med Geniet
2. Receivcd for publicittion;Acccptcd for publication 14 Decembcr,1987
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1. Role of thyroid hormones in craniofacial development;Nature Reviews Endocrinology;2020-01-23
2. Genome rearrangements in patients with blepharophimosis, mental retardation and hypothyroidism, so-called Young-Simpson syndrome;Clinical Genetics;2009-08
3. A clinical and genetic study of the Say/Barber/Biesecker/Young-Simpson type of Ohdo syndrome;Clinical Genetics;2008-09-16
4. Young–Simpson syndrome (YSS), a variant of del(1)(p36) syndrome?;American Journal of Medical Genetics Part A;2008
5. Congenital Hypothyroidism in Young-Simpson Syndrome;Journal of Pediatric Endocrinology and Metabolism;2008-01
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