Trisomy 8p: unusual origin detected by fluorescence in situ hybridization
- 1 May 1992
- journal article
- case report
- Published by Springer Nature in Human Genetics
- Vol. 89 (3) , 307-310
- https://doi.org/10.1007/bf00220547
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Prenatal diagnosis of a partial 8pPrenatal Diagnosis, 1990
- TRISOMY-8P BY MALSEGREGATION OF A T(5-8) (P15-P11)MAT IN A CASE OF XY PURE GONADAL-DYSGENESIS1988
- Cytogenetic Analysis by In Situ Hybridization with Fluorescently Labeled Nucleic Acid ProbesCold Spring Harbor Symposia on Quantitative Biology, 1986
- Controlled silver-staining of nucleolus organizer regions with a protective colloidal developer: a 1-step methodCellular and Molecular Life Sciences, 1980
- Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8pHuman Genetics, 1980
- Complete and partial trisomy of different segments of chromosome 8: case reports and reviewClinical Genetics, 1979
- Trisomy 8p due to the 3:1 segregation of the balanced translocation t(8;15)matHuman Genetics, 1979
- REPORT OF A TRISOMY-8P INFANT WITH CARRIER FATHER1978
- A case of patient with 46, XY, Ep+mat.1974
- A Human Family Suggesting Evidence for Centric Fission and Stability of a Telocentric ChromosomeHuman Heredity, 1972