Mohr syndrome (oro-facial-digital syndrome II) - a familial case with different phenotypic findings-Reference-Cited by-同舟云学术

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Mohr syndrome (oro-facial-digital syndrome II) - a familial case with different phenotypic findings

Published:2008-06-28 Issue:6 Volume:48 Page:304-307
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Prpić Igor,Ćekada Senija,Franulović Jadranka

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1995.tb04114.x/fullpdf

Reference22 articles.

1. Orofacio-digital syndromes I, and II: radiological methods for diagnosis and clinical variations;Anneren;Clin Genet,1984

2. Abnormalities of the cerebellum in oro-facio-digital syndrome II (Mohr syndrome);Anneren;Clin Genet,1990

3. A female infant with features of Mohr and Majewski syndromes: variable expression, a genetic compound, or distinct entity;Baraitser;J Med Genet,1983

4. The oro-facial-digital (OFD) syndromes;Baraitser;J Med Genet,1986

5. Oro-facial-digital syndrome with mesomelic limb shortening;Burn;J Med Genet,1984

Cited by 14 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. Oral-Facial-Digital Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

2. Oral-Facial-Digital Syndrome;Atlas of Genetic Diagnosis and Counseling;2015

3. Oral–Facial–Digital Syndrome;Atlas of Genetic Diagnosis and Counseling;2012

4. Syndromes;Ultrasound of Fetal Syndromes;2008

5. Buccal Anomalies, Cephalometric Analysis and Genetic Study of Two Sisters with Orofaciodigital Syndrome Type I;The Cleft Palate-Craniofacial Journal;2007-11

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