Central nervous system malformations in oral-facial-digital syndrome, type 1 [1]

American Journal of Medical Genetics

Volumn 136 A, Issue 2, 2005, Pages 218-

  Holub, Margareta ^a   Bodamer, Olaf A ^a   Potocki, Lorraine ^b,c  

^a ST ANNA CHILDREN S HOSPITAL   (Austria)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c TEXAS CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BRAIN ARACHNOID CYST; CENTRAL NERVOUS SYSTEM MALFORMATION; CHILD DEVELOPMENT; CORPUS CALLOSUM AGENESIS; DYSOSTOSIS; GRAY MATTER; HUMAN; LETTER; MAJOR CLINICAL STUDY; MENTAL RETARDATION MALFORMATION SYNDROME; NEUROIMAGING; NEUROPATHOLOGY; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; SEX RATIO; X CHROMOSOME DOMINANT DISORDER;

ABNORMALITIES, MULTIPLE; BRAIN; HUMANS; MENTAL RETARDATION; OROFACIODIGITAL SYNDROMES;

EID: 22044455716     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30751     Document Type: Letter

References (2)

1. Ernes RD, Ponting CP. 2001. A new sequence motif linking lissencephaly, Treacher Collins and oral-facial-digital type 1 syndromes, microtubule dynamics and cell migration. Hum Mol Genet 10:2813-2820.
2. Gorlin RJ, Cohen MM, Jr., Hennekam RCM. 2001. Syndromes of the head and neck. 4th edn. New York: Oxford University Press.