A physical map of the mouse shaker-2 region contains many of the genes commonly deleted in Smith-Magenis syndrome (de117p11.2p11.2)

Genomics

Volumn 55, Issue 3, 1999, Pages 348-352

  Probst, Frank J ^a   Chen, Ken Shiung ^b   Zhao, Qi ^b,c   Wang, Aihui ^d,e   Friedman, Thomas B ^e   Lupski, James R ^b,f   Camper, Sally A ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT   (United States)

^d MICHIGAN STATE UNIVERSITY   (United States)

^e NATIONAL INSTITUTES OF HEALTH   (United States)

^f TEXAS CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; MESSENGER RNA;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; CHROMOSOME 17P; GENE DELETION; GENE MAPPING; GENETIC MODEL; MOUSE; MULTIPLE MALFORMATION SYNDROME; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME;

ANIMALIA; MURINAE;

EID: 0033083080     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1998.5669     Document Type: Article

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