Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22

Journal of Medical Genetics

Volumn 33, Issue 11, 1996, Pages 952-956

  Dawson, A J ^a   Mears, A J ^b   Chudley, A E ^a   Bech Hansen, T ^c   McDermid, H ^b  

^a UNIVERSITY OF MANITOBA   (Canada)

^b UNIVERSITY OF ALBERTA   (Canada)

^c UNIVERSITY OF CALGARY   (Canada)

Author keywords

Adjacent 1 segregation; der(22)t(11; 22); Maternal heterodisomy

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; CHILD; CHROMOSOME 11; CHROMOSOME 22; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHROMOSOME PAINTING; CHROMOSOME TRANSLOCATION 11; CONTROLLED STUDY; DISOMY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MAPPING; GENE SEGREGATION; GERM LINE; GROWTH RETARDATION; HETEROZYGOTE; HUMAN; HUMAN CELL; KARYOTYPE; MALE; MEIOSIS; MENTAL DEFICIENCY; NEWBORN; NONDISJUNCTION; PHENOTYPE; PRIORITY JOURNAL; PROGENY; RECIPROCAL CHROMOSOME TRANSLOCATION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SUPERNUMERARY CHROMOSOME; TRISOMY; VARIABLE NUMBER OF TANDEM REPEAT;

EID: 0029839166     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.33.11.952     Document Type: Article

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