Shprintzen-goldberg syndrome: A clinical analysis

American Journal of Medical Genetics

Volumn 76, Issue 3, 1998, Pages 202-212

  Greally, Marie T ^a   Carey, John C ^b   Milewicz, Dianna M ^c   Hudgins, Louanne ^d   Goldberg, Rosalie B ^e   Shprintzen, Robert J ^e   Cousineau, Anthony J ^f   Smith Jr , Wilbur L ^g   Judisch, G Frank ^h   Hanson, James W ^g  

^a ARABIAN GULF UNIVERSITY   (Bahrain)

^b UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

^c UNIVERSITY OF TEXAS   (United States)

^d UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^e MONTEFIORE MEDICAL CENTER   (United States)

^f Department of Pediatrics   (United States)

^g UNIVERSITY OF IOWA   (United States)

^h UNIVERSITY OF IOWA   (United States)

Author keywords

C1 C2 abnormality; Chiari I brain malformation; Craniosynostosis; Fibrillin 1; Marfanoid habitus; Mental retardation; Shprintzen Goldberg syndrome; Transforming growth factor beta

Indexed keywords

FIBRILLIN; TRANSFORMING GROWTH FACTOR BETA;

ARNOLD CHIARI MALFORMATION; ARTICLE; CLINICAL ARTICLE; CRANIOFACIAL MALFORMATION; CRANIOFACIAL SYNOSTOSIS; DIFFERENTIAL DIAGNOSIS; FEMALE; HUMAN; INFANT; MALE; MARFAN SYNDROME; MENTAL RETARDATION MALFORMATION SYNDROME; MULTIPLE MALFORMATION SYNDROME; PRIORITY JOURNAL; SHPRINTZEN GOLDBERG SYNDROME; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; CHILD; CRANIOSYNOSTOSES; FEMALE; FUNNEL CHEST; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MARFAN SYNDROME; MICROFILAMENT PROTEINS; SYNDROME;

EID: 0032546209     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980319)76:3<202::AID-AJMG2>3.0.CO;2-S     Document Type: Article

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