Prenatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization

Prenatal Diagnosis

Volumn 17, Issue 9, 1997, Pages 871-873

  Tardy, Erika P ^a   Tóth, András ^a   Kosztolányi, György ^b  

^a Haynal Imre Medical University   (Hungary)

^b UNIVERSITY OF PÉCS   (Hungary)

Author keywords

Down syndrome; FISH; Partial trisomy 21; Pericentric inversion; Prenatal cytogenetics

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHORION VILLUS SAMPLING; CHROMOSOME 21; CLINICAL FEATURE; CYTOGENETICS; DOWN SYNDROME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MOTHER; PARTIAL TRISOMY; PERICENTRIC CHROMOSOME INVERSION; PRIORITY JOURNAL;

ADULT; CHORIONIC VILLI SAMPLING; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 21; DOWN SYNDROME; FEMALE; FETAL DISEASES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INVERSION, CHROMOSOME; PREGNANCY; PRENATAL DIAGNOSIS; TRISOMY;

EID: 1842326220     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199709)17:9<871::AID-PD140>3.0.CO;2-3     Document Type: Article

References (3)

1. Biesecker, L.G., Rosenberg, M., Dziadzio, L., Ledbetter, D.H., Ning, Y., Sarneso, C., Rosenbaum, K. (1995). Detection of a subtle rearrangement of chromosome 22 using molecular techniques, Am. J. Hum. Genet., 58, 389-394.
2. Matsumoto, N., Niikawa, N., Mikawa, M. (1995). Confirmation of Down syndrome critical region by FISH analysis in a patient with add(21)(p11), Am. J. Med. Genet., 59, 521-522.
3. Pinkel, D., Weier, H.U.G., Grifo, J., Cohen, J. (1988). Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4, Proc. Natl. Acad. Sci. USA, 85, 9138-9142.