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10.1101/cshperspect.a011783 http://scihub22266oqcxt.onion/10.1101/cshperspect.a011783 C3784812!3784812 !23813607     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=23813607 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\23813607 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Cold+Spring+Harb+Perspect+Med 2013 ; 3 (10 ): a011783 Nephropedia Template TP {{tp|p=23813607 |t=2013. The natural history of sickle cell disease |pdf=|usr=}}{{23813607 }} gab.com Text The natural history of sickle cell disease JO: Cold Spring Harb Perspect Med http://www.kidney.de/pget.php?&tw=1&pmid=23813607 #FOAvip The term sickle cell disease embraces a group of genetic conditions in which pathology results from the inheritance of the sickle cell gene either homozygously or as a double heterozygote with another interacting gene. The spectrum of resulting conditions is therefore influenced by the geography of individual hemoglobin genes, but in most populations, the commonest genotype at birth is homozygous sickle cell (SS) disease. Because this genotype generally manifests a greater mortality, the relative proportion of sickle cell genotypes is influenced by age as well as the geographical distribution of individual genes. Twit Text FOAVip The natural history of sickle cell disease ????Cold Spring Harb Perspect Med http://www.kidney.de/pget.php?&tw=1&pmid=23813607 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=23813607 #FOAvip English Wikipedia <ref>{{Cite pmid|23813607 }}</ref> The natural history of sickle cell disease #MMPMID23813607 Serjeant GR Cold Spring Harb Perspect Med 2013[Oct]; 3 (10 ): a011783 PMID23813607 show ga The term sickle cell disease embraces a group of genetic conditions in which pathology results from the inheritance of the sickle cell gene either homozygously or as a double heterozygote with another interacting gene. The spectrum of resulting conditions is therefore influenced by the geography of individual hemoglobin genes, but in most populations, the commonest genotype at birth is homozygous sickle cell (SS) disease. Because this genotype generally manifests a greater mortality, the relative proportion of sickle cell genotypes is influenced by age as well as the geographical distribution of individual genes. |Adult [MESH] |Africa/ethnology [MESH] |Anemia, Sickle Cell/ethnology/*genetics/prevention & control [MESH] |Cause of Death [MESH] |Child [MESH] |Child, Preschool [MESH] |Environmental Health [MESH] |Fetal Hemoglobin/physiology [MESH] |Genotype [MESH] |Geography, Medical [MESH] |Hemoglobins/genetics [MESH] |Homozygote [MESH] |Humans [MESH] |India/ethnology [MESH] |Indian Ocean/ethnology [MESH] |Infant [MESH]The natural history of sickle cell disease (epmc).pdf DeepDyve Pubget Overpricing