نتایج جستجو برای: y microdeletion

تعداد نتایج: 495553  

2012
Md A Mohd Fadley Azli Ismail Thong Meow Keong Narazah Mohd Yusoff Zubaidah Zakaria

INTRODUCTION Chromosomal aberrations of chromosome 16 are uncommon and submicroscopic deletions have rarely been reported. At present, a cytogenetic or molecular abnormality can only be detected in 55% of Rubinstein-Taybi syndrome patients, leaving the diagnosis in 45% of patients to rest on clinical features only. Interestingly, this microdeletion of 16 p13.3 was found in a young child with an...

Journal: :Molecular medicine 2011
Eric Pasmant Julien Masliah-Planchon Pascale Lévy Ingrid Laurendeau Nicolas Ortonne Béatrice Parfait Laurence Valeyrie-Allanore Karen Leroy Pierre Wolkenstein Michel Vidaud Dominique Vidaud Ivan Bièche

Patients with NF1 microdeletion develop more neurofibromas at a younger age, and have an increased risk of malignant peripheral nerve sheath tumors (MPNSTs). We postulated that the increased risk of malignancy could be due to inactivation, in addition to NF1, of a second tumor suppressor gene located in the typical 1.4-Mb microdeletion found in most of the microdeleted patients. We investigated...

2014
Jos I M Egger Willem M A Verhoeven Wim Verbeeck Nicole de Leeuw

The 16p11.2 microdeletion syndrome is characterized by a wide range of phenotypic expressions and is frequently associated with developmental delay, symptoms from the autism spectrum, epilepsy, congenital anomalies, and obesity. These phenotypes are often related to a proximal 16p11.2 deletion of approximately 600 kb (BP4-BP5) that includes the SH2B1 gene that is reported to be causative for mo...

Journal: :JCI insight 2016
Hani Bagheri Chansonette Badduke Ying Qiao Rita Colnaghi Iga Abramowicz Diana Alcantara Christopher Dunham Jiadi Wen Robert S Wildin Malgorzata J M Nowaczyk Jennifer Eichmeyer Anna Lehman Bruno Maranda Sally Martell Xianghong Shan Suzanne M E Lewis Mark O'Driscoll Cheryl Y Gregory-Evans Evica Rajcan-Separovic

The 2p15p16.1 microdeletion syndrome has a core phenotype consisting of intellectual disability, microcephaly, hypotonia, delayed growth, common craniofacial features, and digital anomalies. So far, more than 20 cases of 2p15p16.1 microdeletion syndrome have been reported in the literature; however, the size of the deletions and their breakpoints vary, making it difficult to identify the candid...

Journal: :Biological psychiatry 2014
Kim Fejgin Jacob Nielsen Michelle R Birknow Jesper F Bastlund Vibeke Nielsen Jes B Lauridsen Hreinn Stefansson Stacy Steinberg Helge B D Sorensen Troels E Mortensen Peter H Larsen Ib V Klewe Søren V Rasmussen Kari Stefansson Thomas M Werge Pekka Kallunki Kenneth V Christensen Michael Didriksen

BACKGROUND Genome-wide scans have uncovered rare copy number variants conferring high risk of psychiatric disorders. The 15q13.3 microdeletion is associated with a considerably increased risk of idiopathic generalized epilepsy, intellectual disability, and schizophrenia. METHODS A 15q13.3 microdeletion mouse model (Df[h15q13]/+) was generated by hemizygous deletion of the orthologous region a...

Journal: :JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH 2018

Journal: :Human reproduction 2002
Robert D Oates Sherman Silber Laura G Brown David C Page

BACKGROUND Severe spermatogenic compromise may be the result of a Y-chromosomal deletion of the AZFc region. Prior studies are limited to relatively small numbers of AZFc-deleted men. In this study, we have fully characterized 42 infertile men with a Y chromosome microdeletion strictly confined to the AZFc region, and we report on 18 children conceived through the use of ICSI. METHODS A total...

Journal: :Pediatrics 2001

This set of guidelines is designed to assist the pediatrician to care for children with Williams syndrome diagnosed by clinical features and with regional chromosomal microdeletion confirmed by fluorescence in situ hybridization.

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