نتایج جستجو برای: chromosome 10q

تعداد نتایج: 119424  

2015
Ponnila S Marinescu Devereux N Saller W Tony Parks Svetlana A Yatsenko Aleksandar Rajkovic

We present the prenatal case of a 12.5-Mb duplication involving 6q25-qter and a 12.2-Mb deletion encompassing 10q26-qter diagnosed by aCGH, while conventional karyotype showed normal results. The genotype-phenotype correlation between individual microarray and clinical findings adds to the emerging atlas of chromosomal abnormalities associated with specific prenatal ultrasound abnormalities.

Journal: :Rheumatology 2007
K W Carter A Pluzhnikov A E Timms C Miceli-Richard C Bourgain B P Wordsworth H Jean-Pierre N J Cox L J Palmer M Breban J D Reveille M A Brown

OBJECTIVE Ankylosing spondylitis (AS) is a debilitating chronic inflammatory condition with a high degree of familiality (lambda(s) = 82) and heritability (>90%) that primarily affects spinal and sacroiliac joints. Whole genome scans for linkage to AS phenotypes have been conducted, although results have been inconsistent between studies and all have had modest sample sizes. One potential solut...

Journal: :Hypertension 2002
Richard S Cooper Amy Luke Xiaofeng Zhu Donghui Kan Adebowale Adeyemo Charles Rotimi Nourdine Bouzekri Ryk Ward

An understanding of the genetic influences on hypertension would help unravel the pathophysiology of this complex disorder and improve our understanding of causal mechanisms. Contemporary technology makes it possible to examine enough genetic markers to support a generalized search across the entire genome for candidate regions. In the present study, a family set was recruited from southwest Ni...

Journal: :Journal of medical genetics 1993
S A Farrell W Szymonowicz G Chow A M Summers

A new case of a deletion of 10q23 is described. Only two other deletions involving this region have been previously noted. A review of clinical features of these three children did not show a distinct pattern of dysmorphic features. Other interstitial deletions of 10q are listed.

Journal: :Neuro-oncology 2017
Martin J van den Bent Michael Weller Patrick Y Wen Johan M Kros Ken Aldape Susan Chang

The 2007 World Health Organization (WHO) classification of brain tumors did not use molecular abnormalities as diagnostic criteria. Studies have shown that genotyping allows a better prognostic classification of diffuse glioma with improved treatment selection. This has resulted in a major revision of the WHO classification, which is now for adult diffuse glioma centered around isocitrate dehyd...

2016
Eduard Yakubov Ali Ghoochani Rolf Buslei Michael Buchfelder Ilker Y. Eyüpoglu Nicolai Savaskan

Cowden syndrome (CS) is clinically presented by multiple hamartomas, often with mucocutaneous lesions, goiter, breast cancer and gastrointestinal polyps. CS is a genetic disorder of autosomal dominant inheritance and is one distinct syndrome of the phosphatase and tensin homolog on chromosome 10 (PTEN) hamartoma tumor spectrum. Noteworthy, PTEN germline mutations are related to a wide range of ...

Journal: :Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2010
Barbara S Paugh Chunxu Qu Chris Jones Zhaoli Liu Martyna Adamowicz-Brice Junyuan Zhang Dorine A Bax Beth Coyle Jennifer Barrow Darren Hargrave James Lowe Amar Gajjar Wei Zhao Alberto Broniscer David W Ellison Richard G Grundy Suzanne J Baker

PURPOSE To define copy number alterations and gene expression signatures underlying pediatric high-grade glioma (HGG). PATIENTS AND METHODS We conducted a high-resolution analysis of genomic imbalances in 78 de novo pediatric HGGs, including seven diffuse intrinsic pontine gliomas, and 10 HGGs arising in children who received cranial irradiation for a previous cancer using single nucleotide p...

Journal: :Archives of Disease in Childhood 1997

Journal: :Journal of medical genetics 2005
T Eggermann E Meyer C Obermann I Heil H Schüler M B Ranke K Eggermann H A Wollmann

BACKGROUND Silver-Russell syndrome (SRS) is a heterogeneous malformation syndrome characterised by intrauterine and postnatal growth retardation (IUGR, PGR) and dysmorphisms. The basic causes are unknown, however in approximately 10% of patients a maternal uniparental disomy (UPD) of chromosome 7 or chromosomal aberrations can be detected. Four growth retarded children, two with SRS-like featur...

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