A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: The t(8;22)(q24.13;q11.21)

American Journal of Human Genetics

Volumn 87, Issue 2, 2010, Pages 209-218

  Sheridan, Molly B ^a   Kato, Takema ^b   Haldeman Englert, Chad ^c   Jalali, G Reza ^a   Milunsky, Jeff M ^d   Zou, Ying ^d   Klaes, Ruediger ^e   Gimelli, Georgio ^f   Gimelli, Stefania ^g   Gemmill, Robert M ^h   Drabkin, Harry A ^h   Hacker, April M ^a   Brown, Julia ^a   Tomkins, David ^a   Shaikh, Tamim H ⁱ   Kurahashi, Hiroki ^b   Zackai, Elaine H ^a,j   Emanuel, Beverly S ^a,j  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b FUJITA HEALTH UNIVERSITY   (Japan)

^c WAKE FOREST SCHOOL OF MEDICINE   (United States)

^d BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e Mannheim Center for Human Genetics   (Germany)

^f G GASLINI INSTITUTE   (Italy)

^g GENEVA UNIVERSITY HOSPITALS   (Switzerland)

^h MEDICAL UNIVERSITY OF SOUTH CAROLINA   (United States)

ⁱ Children's Hospital Colorado   (United States)

^j UNIVERSITY OF PENNSYLVANIA   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME BREAKAGE; CHROMOSOME IDENTIFICATION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CONGENITAL MALFORMATION; DNA DETERMINATION; GAMETOGENESIS; HUMAN; HUMAN CELL; INTELLECTUAL IMPAIRMENT; MALE; MEIOSIS; NONDISJUNCTION; NORMAL HUMAN; PALINDROME MEDIATED RECURRENT TRANSLOCATION; PRIORITY JOURNAL; SEMEN ANALYSIS; SKELETON MALFORMATION;

ADOLESCENT; ADULT; AT RICH SEQUENCE; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; GENE DOSAGE; GENOTYPE; HEALTH; HUMANS; INVERTED REPEAT SEQUENCES; MALE; MEIOSIS; MOLECULAR SEQUENCE DATA; NONDISJUNCTION, GENETIC; PHENOTYPE; SEQUENCE ANALYSIS, DNA; SPERMATOGENESIS; SPERMATOZOA; TRANSLOCATION, GENETIC;

EID: 77955570109     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajhg.2010.07.002     Document Type: Article

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