نتایج جستجو برای: homozygosity mapping

تعداد نتایج: 200921  

Journal: : 2021

Homozygosity of Sex Determination Locus and It’s Correlation with Population Honey Production Honeybee (Apis Mellifera Meda) Populations in West-Azerbaijan Kurdistan Provinces

Journal: :Cancer research 1987
W F Benedict E S Srivatsan C Mark A Banerjee R S Sparkes A L Murphree

Sixteen retinoblastomas were examined with chromosome 13 polymorphic probes to determine the frequency of homozygosity for the chromosome in the tumors. Each of the tumors had two cytogenetically normal appearing No. 13 chromosomes. Nontumorous cells from the same patients were heterozygous for the various polymorphic chromosome 13 probes used. At least partial homozygosity for a single chromos...

Journal: :Human mutation 2008
Edgar A Otto Juliana Helou Susan J Allen John F O'Toole Eric L Wise Shazia Ashraf Massimo Attanasio Weibin Zhou Matthias T F Wolf Friedhelm Hildebrandt

Nephronophthisis (NPHP), an autosomal recessive kidney disease, is the most frequent genetic cause of chronic renal failure in the first three decades of life. Mutations in eight genes (NPHP1-8) have been identified. We here describe a combined approach for mutation screening of NPHP1, NPHP2, NPHP3, NPHP4, and NPHP5 in a worldwide cohort of 470 unrelated patients with NPHP. First, homozygous NP...

2012
Hsin-Chou Yang Lun-Ching Chang Yu-Jen Liang Chien-Hsing Lin Pei-Li Wang

Rheumatoid arthritis (RA) is a chronic inflammatory disorder with a polygenic mode of inheritance. This study examined the hypothesis that runs of homozygosity (ROHs) play a recessive-acting role in the underlying RA genetic mechanism and identified RA-associated ROHs. Ours is the first genome-wide homozygosity association study for RA and characterized the ROH patterns associated with RA in th...

Journal: :JAMA 2008
Guillaume Assié Thomas LaFramboise Petra Platzer Charis Eng

CONTEXT Cancer is a multigenic disease resulting from both germline susceptibility and somatic events. While studying loss of heterozygosity (LOH) in cancer tissues, we anecdotally observed a low frequency of heterozygosity in cancer patients compared with controls, raising the question whether homozygosity could play a role in cancer predisposition. OBJECTIVES To determine the frequency of g...

Journal: :Journal of medical genetics 2002
C Thauvin-Robinet V El Ghouzzi W Chemaitilly N Dagoneau O Boute G Viot A Mégarbané A Sefiani A Munnich M Le Merrer V Cormier-Daire

Dyggve-Melchior-Clausen syndrome (DMC) is an autosomal recessive condition characterised by short trunk dwarfism, scoliosis, microcephaly, coarse facies, mental retardation, and characteristic radiological features. X rays show platyspondyly with double vertebral hump, epiphyseal dysplasia, irregular metaphyses, and a characteristic lacy appearance of the iliac crests. Electron microscopy of ch...

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