Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies

Journal of Human Genetics

Volumn 44, Issue 2, 1999, Pages 85-90

  Wakui, Keiko ^a   Tanemura, Mitsuyo ^b   Suzumori, Kaoru ^b   Hidaka, Eiko ^a   Ishikawa, Masayo ^a   Kubota, Takeo ^a   Fukushima, Yoshimitsu ^a  

^a SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NAGOYA CITY UNIV MEDICAL SCHOOL   (Japan)

Author keywords

Chromosome rearrangement; Cryptic translocation; Fluorescence in situ hybridization (FISH); Genetic counseling; Prenatal diagnosis; Telomeric probe; Two color FISH; Whole chromosome painting probe

Indexed keywords

ARTICLE; CHROMOSOME G BAND; CHROMOSOME PAINTING; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; CLINICAL ARTICLE; COLOR; FAMILY STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MULTIPLE MALFORMATION SYNDROME; PRENATAL DIAGNOSIS; RECURRENT ABORTION; TELOMERE;

ABNORMALITIES, MULTIPLE; ABORTION, HABITUAL; CHROMOSOME BANDING; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; PREGNANCY; PRENATAL DIAGNOSIS; TELOMERE;

EID: 0033016168     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380050115     Document Type: Article

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