The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey

European Journal of Medical Genetics

Volumn 49, Issue 3, 2006, Pages 207-214

  Karaman, Birsen ^a   Aytan, Melike ^b   Yilmaz, Kader ^a   Toksoy, Guven ^c   Onal, Ebru Perim ^a   Ghanbari, Asadollah ^a   Engur, Ayse ^b   Kayserili, Hulya ^a   Yuksel Apak, Memnune ^a   Basaran, Seher ^a  

^a ISTANBUL UNIVERSITY   (Turkey)

^b PREMED   (Turkey)

^c Zeynep Kamil Women's and Children's Hospital   (Turkey)

Author keywords

Extra structural abnormal chromosomes; Fluorescence in situ hybridization; Prenatal diagnosis; Ring chromosomes; Small supernumerary marker chromosomes; Supernumerary marker chromosome

Indexed keywords

ACCURACY; ARTICLE; CHROMOSOME 15; CHROMOSOME BAND; CHROMOSOME IDENTIFICATION; CHROMOSOME MARKER; CHROMOSOME SATELLITE; CHROMOSOME STRUCTURE; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOGENETICS; DEVELOPMENTAL DISORDER; EUCHROMATIN; EVALUATION; EVIDENCE BASED MEDICINE; FAMILIAL INCIDENCE; FETUS; FETUS KARYOTYPING; FLUORESCENCE IN SITU HYBRIDIZATION; GENE PROBE; GENETIC ANALYSIS; GENETIC COUNSELING; GENETIC SCREENING; HUMAN; INHERITANCE; ISOCHROMOSOME; MATERIALS; PARENT; PRENATAL DIAGNOSIS; PREVALENCE; SUPERNUMERARY CHROMOSOME; TURKEY (REPUBLIC);

CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CYTOGENETIC ANALYSIS; EUCHROMATIN; FEMALE; FETUS; GENETIC COUNSELING; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MATERNAL AGE; PREGNANCY; PRENATAL DIAGNOSIS; TURKEY;

EID: 33744551930     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2005.06.002     Document Type: Article

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