نتایج جستجو برای: y chromosome microdeletion

تعداد نتایج: 604735  

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 2013

It has been established that the Y chromosome carries genes required for spermatogenesis and male fertility. For many decades worldwide screening for gene identification has been conducted in research laboratories. However, it has been a difficult process in identifying such genes (i.e. causative mutations) which could explain the phenotypic variation and could be potentially used as markers fo...

2016
Hojka Gregoric Kumperscak Danijela Krgovic Nadja Kokalj Vokac

Chromosomal abnormalities involving 2q32q33 deletions are very rare and present with a specific phenotype. This case report describes a 37-year-old female patient with 2q32q33 microdeletion syndrome presenting with the characteristic features, but with the addition of secondary cognitive decline. Molecular karyotyping was performed on the patient and her parents. It revealed an 8.6 megabase del...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Dirk Prawitt Thorsten Enklaar Barbara Gärtner-Rupprecht Christian Spangenberg Monika Oswald Ekkehart Lausch Peter Schmidtke Dirk Reutzel Stephan Fees Rob Lucito Maria Korzon Izabela Brozek Janusz Limon David E Housman Jerry Pelletier Bernhard Zabel

We have analyzed several cases of Beckwith-Wiedemann syndrome (BWS) with Wilms' tumor in a familial setting, which give insight into the complex controls of imprinting and gene expression in the chromosome 11p15 region. We describe a 2.2-kbp microdeletion in the H19/insulin-like growth factor 2 (IGF2)-imprinting center eliminating three target sites of the chromatin insulator protein CTCF that ...

Journal: :Hong Kong medical journal = Xianggang yi xue za zhi 2009
Paulina P Y Ng Mary H Y Tang Elizabeth T Lau Lucy K L Ng Ernest H Y Ng P C Tam William S B Yeung P C Ho

OBJECTIVE To report the type and frequency of chromosomal anomalies and Y-microdeletions among Hong Kong Chinese subfertile men with sperm concentrations lower than 5 million/mL. DESIGN. Retrospective study. SETTING A reproductive centre in Hong Kong. PARTICIPANTS A total of 295 Chinese subfertile men who underwent both karyotyping and Y-microdeletion studies from 2000 to 2007 were categori...

Journal: :Human reproduction 2002
C M Luetjens J Gromoll M Engelhardt S Von Eckardstein M Bergmann E Nieschlag M Simoni

BACKGROUND Deletions of the AZF (azoospermia factor) subregions on the Y chromosome are accompanied by a diverse spectrum of spermatogenic disturbances ranging from hypospermatogenesis to total depletion of germ cells causing infertility. The AZF region encodes gene products which are candidates for the genetic control of spermatogenesis. Although it is known which genes are involved, a general...

2014
Shuo Han Juan C. Bournat Anna Mielnik Ajay Nangia Peter N. Schlegel

Dear Sir, Dr Chianese et al. (2013) expressed concerns about their results reported in ‘Y-chromosome microdeletions are not associated with SHOX haploinsufficiency’ and our earlier publication ‘Aberrations in pseudoautosomal regions (PARs) found in infertile men with Y-chromosome microdeletions’ (Jorgez et al., 2011). We wish to respond to several of their statements regarding our work in hopes...

2016
Tímea Margit Szabó Anikó Ujfalusi Beáta Bessenyei Gabriella P. Szabó Katalin Szakszon István Balogh Éva Oláh

15q11-13 chromosome region contains five breakpoints (BP1-BP5). Chromosomal rearrangements are common in this region. The microdeletion of BP1-BP2 region represents the 15q11.2 microdeletion syndrome associating with variable phenotype. We investigated a ten years old boy with hypotony. His motoric functions, speech and intellectual development were delayed. He suffered from epilepsy and showed...

Journal: :Archives of otolaryngology--head & neck surgery 2000
B Arellano R Ramírez Camacho J R García Berrocal M Villamar I del Castillo F Moreno

OBJECTIVE To study a family with inner ear malformations and sensorineural hearing loss. DESIGN Clinical, radiological, and genetic study of the members of a family with different degrees of sensorineural hearing loss. RESULTS The males in the family manifested profound congenital hearing loss with severe inner ear malformations, while the only affected female had progressive hearing loss t...

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