Limb mammary syndrome: A new genetic disorder with mammary hypoplasia, ectrodactyly, and other hand/foot anomalies maps to human chromosome 3q27

American Journal of Human Genetics

Volumn 64, Issue 2, 1999, Pages 538-546

  Van Bokhoven, Hans ^a   Jung, Martin ^b   Smits, Arie P T ^a   Van Beersum, Sylvia ^a   Rüschendorf, Franz ^b   Van Steensel, Maurice ^a   Veenstra, Monique ^a   Tuerlings, Joep H A M ^a   Mariman, Edwin C M ^a   Brunner, Han G ^a   Wienker, Thomas F ^b   Reis, Andre ^b,c   Ropers, Hans Hilger ^a,d   Hamel, Ben C J ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

^c HUMBOLDT UNIVERSITY   (Germany)

^d MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DNA BINDING PROTEIN; HIGH MOBILITY GROUP B PROTEIN; NUCLEAR PROTEIN; SOX-2 TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR SOX2;

ANIMAL; ARTICLE; CHROMOSOME 3; CHROMOSOME MAP; EXPERIMENTAL NEOPLASM; FEMALE; FOOT MALFORMATION; GENETIC LINKAGE; GENETICS; HAND MALFORMATION; HUMAN; MALE; MULTIPLE MALFORMATION SYNDROME; MUTATION; PATHOPHYSIOLOGY; PEDIGREE; RADIOGRAPHY; SYNDROME;

ABNORMALITIES, MULTIPLE; ANIMALS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 3; DNA-BINDING PROTEINS; FEMALE; FOOT DEFORMITIES, CONGENITAL; HAND DEFORMITIES, CONGENITAL; HMGB PROTEINS; HUMANS; LINKAGE (GENETICS); MALE; MAMMARY NEOPLASMS, ANIMAL; MUTATION; NUCLEAR PROTEINS; PEDIGREE; SYNDROME; TRANSCRIPTION FACTORS;

EID: 0033071807     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302246     Document Type: Article

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