نتایج جستجو برای: supernumerary marker chromosomes

تعداد نتایج: 200561  

Journal: :The Medical journal of Malaysia 1996
M K Thong V Manonmani I S Norlasiah

The finding of a supernumerary or marker chromosome in a karyotype poses difficulty in genetic counselling. The true incidence and significance of this chromosomal aberration is unknown in Malaysia. We report two patients who presented with supernumerary chromosomes in mosaic Turner syndrome.

2016
Érica Alves Serrano Cristian Araya-Jaime Elkin Y. Suárez-Villota Claudio Oliveira Fausto Foresti

Characidium gomesi Travasso, 1956 specimens from the Pardo River have up to four heterochromatic supernumerary chromosomes, derived from the sex chromosomes. To access the meiotic behavior and distribution of an active chromatin marker, males and females of Characidium gomesi with two or three B chromosomes were analyzed. Mitotic chromosomes were characterized using C-banding and FISH with B ch...

Journal: :Journal of Korean Medical Science 2003
Hee Yeon Woo Hyun Jung Cho Sun Young Kong Hee Jin Kim Hyun Bae Jeon Eun Chi Kim Hyosoon Park Young Jae Kim Sun Hee Kim

The identification of marker chromosomes is important for genetic counseling. However, the origin or composition can rarely be defined with conventional cytogenetic technique alone. In this study, we investigated the incidences and types of marker chromosomes in Korean patients and attempted to establish a cost-effective diagnostic approach for marker chromosomes. We reviewed the karyotypes of ...

Journal: :American journal of medical genetics 2000
E D Austin-Ward S Castillo Y Dragnic P Sanz S Salazar J H Knoll

Marker chromosomes present a problem in genetic counseling because there are often no clear phenotype-karyotype correlations. We present the clinical findings in a patient who is mosaic for a supernumerary marker chromosome 20 determined by fluorescence in situ hybridization (FISH) and compare these findings to others reported in the literature.

Journal: :Journal of medical genetics 1998
S R Ghaffari E Boyd J M Connor A M Jones J L Tolmie

We report the use of comparative genomic hybridisation (CGH) to define the origin of a supernumerary ring chromosome which conventional cytogenetic banding and fluorescence in situ hybridisation (FISH) methods had failed to identify. Targeted FISH using whole chromosome 19 library arm and site specific probes then confirmed the CGH results. This study shows the feasibility of using CGH for the ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید