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10.3233/PGE-12038 http://scihub22266oqcxt.onion/10.3233/PGE-12038 C5020949!5020949!27625830     free     free     free Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 215.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Pediatr+Genet 2012 ; 1 (4): 239-42 Nephropedia Template TP {{tp|p=27625830|t=2012. Different chromosome Y abnormalities in a case with short stature |pdf=|usr=}}{{27625830}} gab.com Text Different chromosome Y abnormalities in a case with short stature JO: J Pediatr Genet http://www.kidney.de/pget.php?&tw=1&pmid=27625830 #FOAvip We report a case with different chromosome Y abnormalities. Case was an 11-year-old boy, who was diagnosed with short stature, referred to laboratory of human medical genetics laboratory for genetic evaluation. Chromosomal analysis of the case was carried out on peripheral blood lymphocyte culture. Classic cytogenetic analysis (G and C banding) was confirmed by using fluorescence in situ hybridization analysis (FISH) technique. Cytogenetic and FISH analysis showed a mosaic 46,X,i(Yq)/45,X/47,X,i(Yq)x2/47,XYY karyotype. Case, which was found interesting due to its rarity, is discussed with its clinical features and cytogenetic results, in the light of relevant source information. This case underlines the importance of karyotyping patients with unexplained short stature. This clinical report also will be helpful in defining the phenotypic range associated with these karyotypes. Twit Text FOAVip Different chromosome Y abnormalities in a case with short stature ????J Pediatr Genet http://www.kidney.de/pget.php?&tw=1&pmid=27625830 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27625830 #FOAvip English Wikipedia <ref>{{Cite pmid|27625830}}</ref> Different chromosome Y abnormalities in a case with short stature #MMPMID27625830 Balkan M; Fidanboy M; Özbek MN; Alp MN; Budak T J Pediatr Genet 2012[Dec]; 1 (4): 239-42 PMID27625830show ga We report a case with different chromosome Y abnormalities. Case was an 11-year-old boy, who was diagnosed with short stature, referred to laboratory of human medical genetics laboratory for genetic evaluation. Chromosomal analysis of the case was carried out on peripheral blood lymphocyte culture. Classic cytogenetic analysis (G and C banding) was confirmed by using fluorescence in situ hybridization analysis (FISH) technique. Cytogenetic and FISH analysis showed a mosaic 46,X,i(Yq)/45,X/47,X,i(Yq)x2/47,XYY karyotype. Case, which was found interesting due to its rarity, is discussed with its clinical features and cytogenetic results, in the light of relevant source information. This case underlines the importance of karyotyping patients with unexplained short stature. This clinical report also will be helpful in defining the phenotypic range associated with these karyotypes. äDifferent chromosome Y abnormalities in a case with short stature (epmc).pdf DeepDyve Pubget Overpricing