A unique case of der(11)t(11;22),-22 arising from 3:1 segregation of a maternal t(11;22) in a family with co-segregation of the translocation and breast cancer

Prenatal Diagnosis

Volumn 25, Issue 8, 2005, Pages 683-686

  Jobanputra, Vaidehi ^a   Chung, Wendy K ^a   Hacker, April M ^b   Emanuel, Beverly S ^b,c   Warburton, Dorothy ^a,d  

^a Och Spine at New York Presbyterian Hospitals   (United States)

^b CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^c UNIVERSITY OF PENNSYLVANIA   (United States)

^d NEW YORK PRESBYTERIAN HOSPITAL   (United States)

Author keywords

3:1 segregation; Breast cancer; t(11; 22); Tertiary monosomy

Indexed keywords

ADULT; ARTICLE; BREAST CANCER; CASE REPORT; CHROMOSOME 11Q; CHROMOSOME 22Q; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; GAMETE; GENE SEGREGATION; GENE TRANSLOCATION; GESTATIONAL AGE; HEART BEAT; HETEROZYGOTE DETECTION; HUMAN; KARYOTYPE 46,XX; KARYOTYPE 46,XY; MELANOMA; POLYMERASE CHAIN REACTION; PREGNANCY TERMINATION; PREMENOPAUSE; PRIORITY JOURNAL; SPONTANEOUS ABORTION;

ABORTION, HABITUAL; ADULT; BREAST NEOPLASMS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MEIOSIS; MONOSOMY; PREGNANCY; TRANSLOCATION, GENETIC;

EID: 23844458270     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.1196     Document Type: Article

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