Clustered 11q23 and 22q11 breakpoints and 3:1 meiotic malsegregation in multiple unrelated t(11;22) families

American Journal of Human Genetics

Volumn 65, Issue 6, 1999, Pages 1595-1607

  Shaikh, Tamim H ^a   Budarf, Marcia L ^a,b   Celle, Livija ^a   Zackai, Elaine H ^a,b   Emanuel, Beverly S ^a,b  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 11; CHROMOSOME 22; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION; FAMILIAL INCIDENCE; FEMALE; GENE CLUSTER; GENE SEGREGATION; HUMAN; MALE; MEIOSIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROGENY;

ROBERTSONIA;

EID: 0033358665     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302666     Document Type: Article

References (49)

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