نتایج جستجو برای: q12

تعداد نتایج: 725  

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2019

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2018

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2018

Journal: :Journal of applied genetics 2005
Maria Lassota Barbara Przełozna Marta Płodzien Monika Bugno Maciej Wnuk Zbigniew Kotylak Ewa Słota

In this case report we present a child with an additional chromosome in the karyotype. The karyotypes of the boy and his parents were analyzed by use of a conventional banding technique (GTG) and fluorescence in situ hybridization (FISH). Probes painting whole chromosomes 12 and 18 were used in FISH. Cytogenetic examination of the parents revealed that his mother was carrying balanced reciproca...

Journal: :Genomics 1999
D Smedley R Hamoudi Y J Lu C Cooper J Shipley

Tandem repeats of a novel, putative, zinc-binding motif (MYM) have been described within the products of two, highly homologous genes: ZNF198/RAMP/FIM and ZNF261/DXS6673E. ZNF198, mapping to 13q11-q12, was recently shown to fuse to the fibroblast growth factor receptor 1 gene in the t(8;13)(p11;q11-q12) rearrangement associated with a stem cell leukemia/lymphoma syndrome. ZNF261 at Xq13.1 is di...

2010
Sang Bong Han Jihyang Lim Yonggoo Kim Hee-Je Kim Kyungja Han

A subgroup of acute leukemia with morphology resembling acute promyelocytic leukemia (APL) shows variant translocations involving RARA and has a different morphology from that of classical APL. The variant APL with t(11;17)(q23;q12); ZBTB16-RARA subgroup has been reported to have leukemic cells with regular nuclei, many granules, absence of Auer rods, an increased number of Pelgeroid neutrophil...

2011
Min Jin Kim Sun Young Cho Gayoung Lim Hoi Soo Yoon Hee Joo Lee Jin-Tae Suh Juhie Lee Woo-In Lee Kyung Sam Cho Tae Sung Park

We present a rare case of microgranular variant acute promyelocytic leukemia (APL) associated with ider(17)(q10)t(15;17)(q22;q12) of an old-age patient. The initial chromosome study showed a 46,XX,del(6)(?q21q25),der(15)t(15;17)(q22;q12),ider(17)(q10)t(15;17)[10]/47,sl,+ider(17)(q10)t(15;17)[3]/46,XX[16]. FISH signals from a dual color dual fusion translocation PML-RARA probe were consistent wi...

2005
Hyun Young Ahn Jong Chul Shin Yeon Hee Kim Hyun Sun Ko In Yang Park Sa Jin Kim Jong Gu Rha Soo Pyung Kim

Congenital diaphragmatic hernia (CDH) is often associated with major anomalies and chromosomal abnormalities. Chromosomal abnormalities are usually detected in 9.5% to 34% of fetuses with CDH prenatally diagnosed and the defect has also been reported in association with multiple syndromes such as Pallister-Killian syndrome, Fryns syndrome, Di George syndrome and Apert syndrome. Among the chromo...

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