New p57(KIP2) mutations in Beckwith-Wiedemann syndrome

Human Genetics

Volumn 100, Issue 5-6, 1997, Pages 681-683

  Hatada, Izuho ^a   Nabetani, Akira ^a   Morisaki, Hiroko ^a   Xin, Zhenghan ^a   Ohishi, Sachiko ^a   Tonoki, Hidefumi ^b   Niikawa, Norio ^c   Inoue, Masahiro ^d   Komoto, Yosuke ^d   Okada, Akira ^d   Steichen, Elisabeth ^e   Ohashi, Hirofumi ^f   Fukushima, Yoshimitsu ^g   Nakayama, Masahiro ^h   Mukai, Tsunehiro ^a  

^a NATIONAL CEREBRAL AND CARDIOVASCULAR CENTER   (Japan)

^b HOKKAIDO UNIVERSITY   (Japan)

^c NAGASAKI UNIVERSITY   (Japan)

^d OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

^e UNIVERSITY OF INNSBRUCK   (Austria)

^f SAITAMA CHILDREN'S MEDICAL CENTER   (Japan)

^g SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^h RESEARCH INSTITUTE FOR MATERNAL AND CHILD HEALTH   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN DEPENDENT KINASE INHIBITOR; CDKN1C PROTEIN, HUMAN; CYCLIN DEPENDENT KINASE INHIBITOR 1C; NUCLEAR PROTEIN;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BECKWITH WIEDEMANN SYNDROME; CHILD; CHROMOSOME 11P; CLINICAL ARTICLE; FEMALE; GENE LOCATION; GENE MUTATION; GENETIC LINKAGE; GENETIC SCREENING; GENOME IMPRINTING; HUMAN; MALE; PRIORITY JOURNAL; UNIPARENTAL DISOMY; AUSTRIA; CHROMOSOME 11; FRAMESHIFT MUTATION; GENETICS; JAPAN; NEWBORN; POINT MUTATION;

AUSTRIA; BECKWITH-WIEDEMANN SYNDROME; CHROMOSOMES, HUMAN, PAIR 11; CYCLIN-DEPENDENT KINASE INHIBITOR P57; FEMALE; FRAMESHIFT MUTATION; GENETIC SCREENING; HUMANS; INFANT, NEWBORN; JAPAN; MALE; NUCLEAR PROTEINS; POINT MUTATION;

EID: 0031284743     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050573     Document Type: Article

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