Small supernumerary marker chromosomes (sSMC) in humans

Cytogenetic and Genome Research

Volumn 107, Issue 1-2, 2004, Pages 55-67

  Liehr, T ^a,b   Claussen, U ^a   Starke, H ^a  

^a Institute of Human Genetics and Anthropology   (Germany)

^b Institut fur Humangenetik und Anthropologie   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ACROCENTRIC CHROMOSOME; CELL CYCLE; CENTROMERE; CHROMOSOME 12Q; CHROMOSOME 15; CHROMOSOME 17; CHROMOSOME 17P; CHROMOSOME 19P; CHROMOSOME 1P; CHROMOSOME 1Q; CHROMOSOME 22; CHROMOSOME 22Q; CHROMOSOME 2P; CHROMOSOME 2Q; CHROMOSOME 3P; CHROMOSOME 4Q; CHROMOSOME 5Q; CHROMOSOME 7P; CHROMOSOME 7Q; CHROMOSOME 8P; CHROMOSOME 9P; CHROMOSOME DUPLICATION; CHROMOSOME MARKER; CHROMOSOME SATELLITE; CHROMOSOME SIZE; CHROMOSOME STRUCTURE; CONFERENCE PAPER; CORRELATION ANALYSIS; DISOMY; DOWN SYNDROME; FAMILIAL DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; FREQUENCY ANALYSIS; HUMAN; KARYOTYPE; MOLECULAR GENETICS; MOSAICISM; NOMENCLATURE; PALLISTER KILLIAN SYNDROME; PHENOTYPE; PRIORITY JOURNAL; PSYCHOMOTOR DISORDER; RING CHROMOSOME; STRUCTURAL CHROMOSOME ABERRATION; SUPERNUMERARY CHROMOSOME; SYNDROME; TRISOMY; TURNER SYNDROME; X CHROMOSOME;

CHROMOSOMES, HUMAN; HUMANS;

FELIS CATUS;

EID: 4344625842     PISSN: 14248581     EISSN: None     Source Type: Journal    
DOI: 10.1159/000079572     Document Type: Conference Paper

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