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http://scihub22266oqcxt.onion/ 8434586/?report=reader!1682134!8434586     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Am+J+Hum+Genet 1993 ; 52 (1): 176-82 Nephropedia Template TP {{tp|p=8434586|t=1993. Constitutional 1p36 deletion in a child with neuroblastoma |pdf=|usr=}}{{8434586}} gab.com Text Constitutional 1p36 deletion in a child with neuroblastoma JO: Am J Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=8434586 #FOAvip We describe a child with dysmorphic features, as well as developmental and growth delay, who developed neuroblastoma at 5 mo of age. Cytogenetic analysis of blood lymphocytes revealed an interstitial deletion of 1p36.1-->1p36.2, which was apparent only with high-resolution banding. Molecular analysis with a collection of polymorphic DNA probes for 1p confirmed an interstitial deletion involving subbands of 1p36. Deletions of this region are a common finding in neuroblastoma cells from patients with advanced stages of disease. Therefore, these results (a) suggest that constitutional deletion of this region predisposed the patient to the development of neuroblastoma and (b) support the localization of a neuroblastoma tumor-suppressor locus to 1p36. Twit Text FOAVip Constitutional 1p36 deletion in a child with neuroblastoma ????Am J Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=8434586 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=8434586 #FOAvip English Wikipedia <ref>{{Cite pmid|8434586}}</ref> Constitutional 1p36 deletion in a child with neuroblastoma #MMPMID8434586 Biegel JA; White PS; Marshall HN; Fujimori M; Zackai EH; Scher CD; Brodeur GM; Emanuel BS Am J Hum Genet 1993[Jan]; 52 (1): 176-82 PMID8434586show ga We describe a child with dysmorphic features, as well as developmental and growth delay, who developed neuroblastoma at 5 mo of age. Cytogenetic analysis of blood lymphocytes revealed an interstitial deletion of 1p36.1-->1p36.2, which was apparent only with high-resolution banding. Molecular analysis with a collection of polymorphic DNA probes for 1p confirmed an interstitial deletion involving subbands of 1p36. Deletions of this region are a common finding in neuroblastoma cells from patients with advanced stages of disease. Therefore, these results (a) suggest that constitutional deletion of this region predisposed the patient to the development of neuroblastoma and (b) support the localization of a neuroblastoma tumor-suppressor locus to 1p36. |*Chromosomes, Human, Pair 1[MESH] |*Gene Deletion[MESH] |Adult[MESH] |Cells, Cultured[MESH] |Chromosome Mapping[MESH] |Female[MESH] |Genes, Tumor Suppressor[MESH] |Genetic Predisposition to Disease[MESH] |Humans[MESH] |Infant, Newborn[MESH] |Karyotyping[MESH] |Male[MESH] |Neuroblastoma/*genetics[MESH]Constitutional 1p36 deletion in a child with neuroblastoma (epmc).pdf DeepDyve Pubget Overpricing