نتایج جستجو برای: chromosome microdeletion

تعداد نتایج: 120218  

Journal: :Journal of medical genetics 2010
S Spengler N Schönherr G Binder H A Wollmann S Fricke-Otto R Mühlenberg B Denecke M Baudis T Eggermann

Silver-Russell syndrome (SRS) is a heterogeneous disorder associated with intrauterine and postnatal growth restriction, body asymmetry, a relative macrocephaly, a characteristic triangular face and further dysmorphisms. In about 50% of patients, genetic/epigenetic alterations can be detected: >38% of patients show a hypomethylation of the IGF2/H19 imprinting region in 11p15, whereas the additi...

2012
Heather C Mefford Jill A Rosenfeld Natasha Shur Anne M Slavotinek Victoria A Cox Raoul C Hennekam Helen V Firth Lionel Willatt Patricia Wheeler Eric M Morrow Joseph Cook Rachel Sullivan Albert Oh Marie T McDonald Jonathan Zonana Kory Keller Mark C Hannibal Susie Ball Jennifer Kussmann Jerome Gorski Susan Zelewski Valerie Banks Wendy Smith Rosemarie Smith Lindsay Paull Kenneth N Rosenbaum David J Amor Joao Silva Allen Lamb Evan E Eichler

BACKGROUND Chromosome 15q24 microdeletion syndrome is a rare genomic disorder characterised by intellectual disability, growth retardation, unusual facial morphology and other anomalies. To date, 20 patients have been reported; 18 have had detailed breakpoint analysis. AIM To further delineate the features of the 15q24 microdeletion syndrome, the clinical and molecular characterisation of fif...

Journal: :Journal of Fertilization: In Vitro - IVF-Worldwide, Reproductive Medicine, Genetics and Stem Cell 2014

Journal: :Clinical genetics 2010
R A Kumar

Genomic disorders involving microdeletions and microduplications have been reported in many individuals with neuropsychiatric disorders such as autism and mental retardation. The recurrent nature of these disorders is often explained by nonallelic homologous recombination (NAHR) mediated by large blocks of highly identical segmental duplications or low copy repeats (LCR). The rapidly growing li...

Journal: :Journal of the American College of Cardiology 2005
Luc M Beauchesne Carole A Warnes Heidi M Connolly Naser M Ammash Martha Grogan Syed M Jalal Virginia V Michels

OBJECTIVES This study was designed to determine the prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies and to assess the clinician's ability to predict the presence or absence of 22q11.2 microdeletion on the basis of clinical features. BACKGROUND It is known that 22q11.2 microdeletion is a chromosomal anomaly with cardiac and extracar...

Journal: :Cytogenetic and genome research 2014
B Y Lee S Y Kim J Y Park E Y Choi D J Kim J W Kim H M Ryu Y H Cho S Y Park J T Seo

Infertile men with azoospermia commonly have associated microdeletions in the azoospermia factor (AZF) region of the Y chromosome, sex chromosome mosaicism, or sex chromosome rearrangements. In this study, we describe an unusual 46,XX and 45,X mosaicism with a rare Y chromosome rearrangement in a phenotypically normal male patient. The patient's karyotype was 46,XX[50]/45,X[25]/46,X,der(Y)(pter...

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