Status of the human malformation map: 2002

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 115, Issue 4, 2002, Pages 205-220

  Carey, John C ^a   Viskochil, David H ^b  

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

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 2; DNA; GROWTH FACTOR; SCLEROPROTEIN; TRANSCRIPTION FACTOR;

BARDET BIEDL SYNDROME; CHONDROGENESIS; CHROMOSOMAL LOCALIZATION; CONGENITAL MALFORMATION; DYSPLASIA; GENE IDENTIFICATION; GENE MAPPING; GENE MUTATION; HIRSCHSPRUNG DISEASE; HUMAN; MOLECULAR CLONING; MORPHOGENESIS; PALLISTER HALL SYNDROME; PHENOTYPE; POLYDACTYLY; PRIORITY JOURNAL; REVIEW; STICKLER SYNDROME; SYNDROME; VAN DER WOUDE SYNDROME; WEBBED NECK;

ABNORMALITIES; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN; FEMALE; HUMANS; MALE; SYNDROME;

JONES;

EID: 0036955306     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10987     Document Type: Review

References (5)

1. Carey JC, Viskochil DH. 1996. Current status of the human malformation map. Birth Defects: Orig Attic Ser 30(1):13-34.
2. th edition. WB. Saunders Company.
3. Jorde LB, Carey JC, Bamshad MJ, White RL. 1999. Medical Genetics. Mosby.
4. OMIM. 2002. web page: www.ncbi.nlm.nih.gov/Omim/
5. Smith R. 2002. Hereditary Deafness. Gene Clinics web page: www.geneclinics.org/www.genetests.org/