The spectrum of mutations in TBX3: Genotype/phenotype relationship in ulnar-mammary syndrome

American Journal of Human Genetics

Volumn 64, Issue 6, 1999, Pages 1550-1562

  Bamshad, M ^a,c   Le, T ^b   Watkins, W S ^b   Dixon, M E ^b   Kramer, B E ^b   Roeder, A D ^b   Carey, J C ^a   Root, S ^d   Schinzel, A ^e   Van Maldergem, L ^f   Gardner, R J M ⁱ   Lin, R C ⁱ   Seidman, C E ⁱ   Seidman, J G ⁱ   Wallerstein, R ^g   Moran, E ^g,h   Sutphen, R ⁱ   Campbell, C E ⁱ   Jorde, L B ^c  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

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

^c SHRINERS HOSPITALS FOR CHILDREN   (United States)

^d UNIVERSITY OF NEW MEXICO   (United States)

^e UNIVERSITY OF ZURICH   (Switzerland)

^f Centre de Genetique Humaine   (Belgium)

^g NEW YORK UNIVERSITY MEDICAL CENTER   (United States)

^h NYU HOSPITAL FOR JOINT DISEASES   (United States)

ⁱ NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; DELETION MUTANT; DNA BINDING; DNA SEQUENCE; FRAMESHIFT MUTATION; GENE MUTATION; GENOTYPE; HUMAN; HUMAN CELL; HUMAN TISSUE; MISSENSE MUTATION; OPEN READING FRAME; PHENOTYPE; PLEIOTROPY; PRIORITY JOURNAL; TATA BOX; ULNAR MAMMARY SYNDROME;

EID: 0033364962     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302417     Document Type: Article

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