Abnormalities of the cerebellum in oro-facio-digital syndrome II (Mohr syndrome)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1990.tb03549.x/fullpdf
Reference19 articles.
1. Oro-facio-digital syndromes I and II: radiological methods for diagnosis and the clinical variations;Annerén;Clin. Genet.,1984
2. The orofaciodigital (OFD) syndromes;Baraister;J. Med. Genet.,1986
3. X-linked recessive inheritance of an oro-facio-digital syndrome with partial expression in females and survival of affected males;Edwards;Clin. Genet.,1988
4. Joubert syndrome: early diagnosis of the behavior phenotype and confirmation by cranial sonography;Edwards;J. Child Neurol.,1988
5. Joubert-Boltshauser syndrome with polydactyly in siblings;Egger;J. Neurol. Neurosurg. Psychiatr.,1982
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2. The Many Faces of Oral-Facial-Digital Syndrome;Balkan Journal of Medical Genetics;2012-01-01
3. Mohr syndrome (oro-facial-digital syndrome II) - a familial case with different phenotypic findings;Clinical Genetics;2008-06-28
4. Ectrodactyly-ectodermal dysplasiaclefting syndrome (EEC): the clinical variation and prenatal diagnosis;Clinical Genetics;2008-06-28
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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