Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome

Cytogenetics and Cell Genetics

Volumn 91, Issue 1-4, 2000, Pages 165-170

  Levy, Brynn ^a   Papenhausen, P R ^b   Tepperberg, J H ^b   Dunn, T M ^a   Fallet, S ^a,c   Magid, M S ^a   Kardon, N B ^a   Hirschhorn, K ^a   Warburton, P E ^a  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^b LABORATORY CORPORATION OF AMERICA   (United States)

^c CHILDREN S HOSPITAL OF NEW JERSEY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNION FLUID CYTOLOGY; ARTICLE; CASE REPORT; CHROMOSOME 10P; CHROMOSOME DUPLICATION; CHROMOSOME INVERSION; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TETRASOMY;

EID: 0034488623     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000056839     Document Type: Article

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