Shprintzen-Goldberg syndrome: Fourteen new patients and a clinical analysis-Reference-Cited by-同舟云学术

Shprintzen-Goldberg syndrome: Fourteen new patients and a clinical analysis

Published:2005 Issue:3 Volume:135A Page:251-262
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Robinson Peter N.,Neumann Luitgard M.,Demuth Stephanie,Enders Herbert,Jung Ursula,König Rainer,Mitulla Beate,Müller Dietmar,Muschke Petra,Pfeiffer Lutz,Prager Bettina,Somer Mirja,Tinschert Sigrid

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference25 articles.

1. Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome

2. Detection of thirty novelFBN1mutations in patients with Marfan syndrome or a related fibrillinopathy

3. Homocystinuria: A new inborn error of Metabolism associated with Mental Deficiency

4. Revised diagnostic criteria for the Marfan syndrome

5. New marfanoid syndrome with craniosynostosis

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