Recommended Pages at jmg.bmj.com
Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion -- Klopocki et al. -- Journal of Medical Genetics
jmg.bmj.com — “Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion -- Klopocki et al. -- Journal of Medical Genetics” View full resource at jmg.bmj.com
Most Recently Shared on December 7, 2011 at 6:00 pm By:
Jon D. Moulton PhD, Active Health Library, Doctor, and Science Enthusiast
Regulation of vertebrate nervous system alternative splicing and development by an SR-related protein. http://t.co/EuLjjLAe #Morpholino
Identification of quantitative trait loci for murine autoimmune pancreatitis -- Asghari et al. 48 (8): 557 -- Journal of Medical Genetics
jmg.bmj.com — “Identification of quantitative trait loci for murine autoimmune pancreatitis -- Asghari et al. 48 (8): 557 -- Journal of Medical Genetics” View full resource at jmg.bmj.com
Most Recently Shared on July 22, 2011 at 1:07 am By:
Identification of quantitative trait loci for murine autoimmune pancreatitis: Conclusions This study has identif... http://bit.ly/qroW8Y
Screening patients referred to a metabolic clinic for lysosomal storage disorders -- Fuller et al. 48 (6): 422 -- Journal of Medical Genetics
jmg.bmj.com — “Fuller, Maria; Tucker, Justin N; Lang, Debbie L; Dean, Caroline J; Fietz, Michael J; Meikle, Peter J; Hopwood, John J” View full resource at jmg.bmj.com
Most Recently Shared on June 2, 2011 at 8:15 pm By:
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Screening patients referred to a metabolic clinic for lysosomal storage disorders. http://bit.ly/kukx1E
Risk of breast cancer in male BRCA2 carriers -- Evans et al. -- Journal of Medical Genetics
jmg.bmj.com — “Evans, D G R; Susnerwala, I; Dawson, J; Woodward, E; Maher, E R; Lalloo, F” View full resource at jmg.bmj.com
Most Recently Shared on February 5, 2011 at 3:15 am By:
Mark Robson Physician, Doctor, Internist, Oncologist, and Hematologist
Sorry about invalid link. Try again. Risk of breast cancer in male BRCA2 carriers http://bit.ly/i91PBD
Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani"Lenz-like non-syndromic oligosyndactyly -- Dimitrov et al. 47 (8): 569 -- Journal of Medical Genetics
jmg.bmj.com — “Dimitrov, Boyan Ivanov; Voet, Thierry; De Smet, Luc; Vermeesch, Joris Robert; Devriendt, Koen; Fryns, Jean-Pierre; Debeer, Philippe” View full resource at jmg.bmj.com
Most Recently Shared on July 24, 2010 at 12:36 pm By:
Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal ... http://bit.ly/aUW2m1
BRCA1, BRCA2 and CHEK2 c.1100 delC mutations in patients with double primaries of the breasts and/or ovaries -- Evans et al. 47 (8): 561 -- Journal of Medical Genetics
jmg.bmj.com — “Evans, D Gareth; Ahmed, Munaza; Bayliss, Stuart; Howard, Emma; Lalloo, Fiona; Wallace, Andrew” View full resource at jmg.bmj.com
Most Recently Shared on July 24, 2010 at 12:36 pm By:
BRCA1, BRCA2 and CHEK2 c.1100 delC mutations in patients with double primaries of the breasts and/or ovaries: This... http://bit.ly/cvNhRm
Constitutional (germline) MLH1 epimutation as an aetiological mechanism for hereditary non-polyposis colorectal cancer -- Hitchins and Ward 46 (12): 793 -- Journal of Medical Genetics
jmg.bmj.com — “Hitchins, M P; Ward, R L” View full resource at jmg.bmj.com
Most Recently Shared on December 2, 2009 at 2:53 am By:
Mark Robson Physician, Doctor, Internist, Oncologist, and Hematologist
Constitutional (germline) MLH1 epimutation as an aetiological mechanism for hereditary non-polyposis colorectal cancer http://bit.ly/4CKtz2
Breast cancer susceptibility variants alter risks in familial disease -- Latif et al. -- Journal of Medical Genetics
jmg.bmj.com — “Latif, Ayse; Hadfield, Kristen D; Roberts, Stephen A; Shenton, Andrew; Lalloo, Fiona; Black, Graeme C M; Howell, Anthony; Evans, D Gareth; Newman, William G” View full resource at jmg.bmj.com
Most Recently Shared on July 28, 2009 at 3:49 pm By:
Mark Robson Physician, Doctor, Internist, Oncologist, and Hematologist
http://bit.ly/H6SwS Manchester group reporting that risk SNPs have risk effects in individuals with family histories of breast cancer
