Deletion mapping of 22q11 in CATCH22 syndrome: Identification of a second critical region [4]

American Journal of Human Genetics

Volumn 58, Issue 6, 1996, Pages 1377-1381

  Kurahashi, H ^a   Nakayama, T ^a   Osugi, Y ^a   Tsuda, E ^a   Masuno, M ^a   Imaizumi, K ^a   Kamiya, T ^a   Sano, T ^a   Okada, S ^a   Nishisho, I ^a  

^a OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CENTROMERE; CHROMOSOME 22Q; CHROMOSOME TRANSLOCATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MAPPING; HEMIZYGOSITY; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALFORMATION SYNDROME; METAPHASE CHROMOSOME; PRIORITY JOURNAL; TELOMERE;

ABNORMALITIES; CELL LINE; CENTROMERE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; SEQUENCE DELETION; SYNDROME;

EID: 0029882855     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

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