Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome

Human Genetics

Volumn 103, Issue 1, 1998, Pages 70-80

  Matsuoka, Rumiko ^a   Kimura, Misa ^a   Scambler, Peter J ^b   Morrow, Bernice E ^c   Imamura, Shin Ichiro ^a   Minoshima, Shinsei ^d   Shimizu, Nobuyoshi ^d   Yamagishi, Hiroyuki ^d   Joh o, Kunitaka ^e   Watanabe, Seiichi ^f   Oyama, Kotaro ^g   Saji, Tsutomu ^h   Ando, Masahiko ^a   Takao, Atsuyoshi ^a   Momma, Kazuo ^a  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d KEIO UNIVERSITY   (Japan)

^e Kyushu Welfare Pension Hospital   (Japan)

^f Tsuchiura Kyodo Hospital   (Japan)

^g IWATE MEDICAL UNIVERSITY   (Japan)

^h TOHO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ANUS ATRESIA; ARTICLE; BRAIN ATROPHY; CARDIOVASCULAR MALFORMATION; CHILD; CHROMOSOME 22Q; CLINICAL EXAMINATION; CONOTRUNCAL ANOMALY FACE SYNDROME; FACE MALFORMATION; FACIAL NERVE PARALYSIS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HEMIZYGOSITY; HUMAN; INFANT; INFECTION SENSITIVITY; INHERITANCE; LIMB MALFORMATION; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; MOLECULAR BIOLOGY; PHENOTYPE; PRIORITY JOURNAL; SCHIZOPHRENIA; SHORT STATURE; THROMBOCYTOPENIA; VOICE;

EID: 0031659846     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050786     Document Type: Article

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