Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome

Genomics

Volumn 79, Issue 2, 2002, Pages 186-196

  Nakabayashi, Kazuhiko ^a   Fernandez, Bridget A ^a,b   Teshima, Ikuko ^a   Shuman, Cheryl ^a   Proud, Virginia K ^c   Curry, Cynthia J ^d   Chitayat, David ^a   Grebe, Theresa ^e   Ming, Jeffrey ^f   Oshimura, Mitsuo ^g   Meguro, Makiko ^g   Mitsuya, Kohzoh ^g   Deb Rinker, Paromita ^a   Herbrick, Jo Anne ^a   Weksberg, Rosanna ^a   Scherer, Stephen W ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b MEMORIAL UNIVERSITY OF NEWFOUNDLAND   (Canada)

^c EASTERN VIRGINIA MEDICAL SCHOOL   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e UNIVERSITY OF ARIZONA   (United States)

^f CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^g TOTTORI UNIVERSITY   (Japan)

Author keywords

FISH mapping; Human chromosome 7; Imprinting; Russell Silver syndrome

Indexed keywords

ALLELISM; ARTICLE; CHROMOSOME 7; CHROMOSOME 7P; CHROMOSOME ABERRATION; CHROMOSOME BREAKAGE; CHROMOSOME DUPLICATION; CHROMOSOME MAP; CHROMOSOME REARRANGEMENT; CHROMOSOME STRUCTURE; FACE DYSMORPHIA; FLUORESCENCE IN SITU HYBRIDIZATION; GENOME IMPRINTING; GROWTH RETARDATION; HUMAN; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PARACENTRIC CHROMOSOME INVERSION; PRIORITY JOURNAL; SHORT STATURE; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY;

EID: 18244389962     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2002.6695     Document Type: Article

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