๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Identification of some marker chromosomes in acute leukemias by fluorescence in situ hybridization

โœ Scribed by Guangping Shi; Hans Josef Weh; Dieter K. Hossfeld


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
403 KB
Volume
11
Category
Article
ISSN
0278-0232

No coin nor oath required. For personal study only.

โœฆ Synopsis


Four patients with acute leukemia are presented in whom conventional karyotypic analysis had revealed complex numerical and structural changes including unidentifiable (marker) chromosomes. It is demonstrated that the application of fluorescence in situ hybridization (FISH) may contribute to the identification of such anomalies.


๐Ÿ“œ SIMILAR VOLUMES


Supernumerary ring chromosome 17 identif
โœ Fagan, Kerry; Edwards, Matthew ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 290 KB ๐Ÿ‘ 2 views

We present a patient with multiple anomalies and severe developmental delay. A small supernumerary ring chromosome was found in 40% of her lymphocyte cells at birth. The origin of the marker chromosome could not be determined by GTG banding, but fluorescent in situ hybridization (FISH) later identif

Minute chromosomal rearrangements detect
โœ Kaoru Suzumori; Mitsuyo Tanemura; Naomi Oya; Nobuhiro Suzumori; Kyoung Chang Kim ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 236 KB ๐Ÿ‘ 2 views

Initial approaches to prenatal diagnosis from fetal karyotyping involved application of standard cytogenetic techniques. However, when fetal samples, such as chorionic villus cells or amniocytes are used, small chromosome rearrangements cannot be easily identified because they lack a distinct bandin

Sex chromosome markers: Characterization
โœ Schwartz, Stuart; Depinet, Theresa W.; Leana-Cox, Julie; Isada, Nelson B.; Karso ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 63 KB ๐Ÿ‘ 2 views

Fluorescence in situ hybridization (FISH) using biotin labeled X-and Y-chromosome DNA probes was utilized in the analysis of 23 sex chromosome-derived markers. Specimens were obtained through prenatal diagnosis, because of a presumptive diagnosis of Ullrich-Turner syndrome, mental retardation, and m

Rapid identification of marker chromosom
โœ Velagaleti, G. V. N.; Tharapel, S. A.; Martens, P. R.; Tharapel, A. T. ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 21 KB ๐Ÿ‘ 2 views

Primed in situ labeling (PRINS) is a relatively new technology with wide-ranging applications in clinical cytogenetics. Using PRINS, we have identified the chromosomal origin of marker chromosomes in three patients. In the first patient with primary amenorrhea, we were able to confirm the marker chr