Mapping of a gene for May-Hegglin anomaly to chromosome 22q

Human Genetics

Volumn 105, Issue 5, 1999, Pages 379-383

  Kunishima, Shinji ^a,b   Kojima, Tetsuhito ^b   Tanaka, Toshihiro ^c   Kamiya, Tadashi ^a   Ozawa, Kazuo ^a   Nakamura, Yusuke ^c   Saito, Hidehiko ^b  

^a JAPANESE RED CROSS SOCIETY   (Japan)

^b NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c UNIVERSITY OF TOKYO   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; DNA MARKER; GLYCOPROTEIN IB;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 22Q; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; FAMILY STUDY; FEMALE; GENE MAPPING; GENETIC LINKAGE; GENETIC RECOMBINATION; HAPLOTYPE; HUMAN; HUMAN CELL; MALE; MAY HEGGLIN ANOMALY; PRIORITY JOURNAL; TANDEM REPEAT; THROMBOCYTE DISORDER;

ADULT; BLOOD PLATELETS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; GENETIC MARKERS; GRANULOCYTES; HUMANS; INCLUSION BODIES; LINKAGE (GENETICS); LOD SCORE; MALE; PEDIGREE; PLATELET GLYCOPROTEIN GPIB-IX COMPLEX; TANDEM REPEAT SEQUENCES; THROMBOCYTOPENIA;

EID: 0032748139     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390051119     Document Type: Article

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