Results 221 to 230 of about 10,401 (233)

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2‐q15

Clinical Genetics, 2009
Ali Muhammad Waryah, Ateequr Rehman, Zubair M Ahmed   +2 more
exaly  

t(15;21)(q15;q22.1)pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring

1996
Dvorah Abeliovich, Judith Dagan, Israela Lerer   +2 more
exaly  

A novel RP2 missense mutation Q158P identified in an X-linked retinitis pigmentosa family impaired RP2 protein stability

Gene, 2019
Yuanfang Ma, Hongmei Mu, Xiukun Cui
exaly  

Chromosome 12q13–q15 translocation breakpoints in solid tumors

Cancer Genetics and Cytogenetics, 1994
openaire   +1 more source

Truncation of αB-Crystallin by the Myopathy-causing Q151X Mutation Significantly Destabilizes the Protein Leading to Aggregate Formation in Transfected Cells

Journal of Biological Chemistry, 2008
Roy A Quinlan
exaly  

Drug pipeline: 2Q15

Nature Biotechnology, 2015
Laura Defrancesco
exaly  

Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24)

Genes Chromosomes and Cancer, 2003
Paola Dal Cin, Bradley J Quade, Stanislawa Weremowicz   +2 more
exaly  

7 4QMez C (4Q151)

2022
exaly  

Absence of HMGIC-LHFP fusion in pulmonary chondroid hamartomas with aberrations involving chromosomal regions 12q13∼q15 and 13q12∼q14

Cancer Genetics and Cytogenetics, 2002
Piere Rogalla, Jorn Bullerdiek
exaly  

The motet section of Bologna Q15 and its ramifying roots

1999
openaire   +1 more source