Growth hormone deficiency in a case of cerebrofaciothoracic syndrome in one of two affected siblings-Reference-Cited by-同舟云学术

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Growth hormone deficiency in a case of cerebrofaciothoracic syndrome in one of two affected siblings

Published:2004 Issue:3 Volume:129A Page:330-330
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kanaka-Gantenbein Christina,Fryssira Helen,Chrousos George,Mastorakos George

Publisher

Wiley

Subject

Genetics (clinical)

Reference3 articles.

1. 2001. Syndromes of the head and neck. 4th edition. New York: Oxford University Press.

2. Cerebro-Facio-Thoracic Dysplasia: Report of Three Cases

Cited by 6 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. Whole-exome sequencing links TMCO1 defect syndrome with cerebro-facio-thoracic dysplasia;European Journal of Human Genetics;2014-01-15

2. An additional case of cerebrofaciothoracic dysplasia associated with Chiari type I malformation;Clinical Dysmorphology;2013-07

3. A new case of cerebro-facio-thoracic dysplasia in a 3-year-old girl with short stature and hypothyroidism;Clinical Dysmorphology;2012-07

4. Spondylocarpotarsal synostosis: Long-term follow-up of a case due toFLNB mutations;American Journal of Medical Genetics Part A;2008

5. Cerebro-facio-thoracic dysplasia: expanding the phenotype;Clinical Dysmorphology;2007-04

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