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C E Jackson

Showing results (171-180 of 180) with videos related to

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Nature Genetics|June 1, 1996
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2D W Johnson, J N Berg, M A Baldwin, et al.
American Journal of Human Genetics|May 1, 1997
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.
QJM : Monthly Journal of the Association of Physicians|September 1, 1996
Clinical studies of multiple endocrine neoplasia type 1 (MEN1)D Trump, B Farren, C Wooding, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.
Blood|June 22, 2001
The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosisS E Straus, E S Jaffe, J M Puck, et al.
Neurology|February 27, 2001
Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathyJ R Mendell, R J Barohn, M L Freimer, et al.
Human Mutation|April 29, 1998
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null allelesC J Gallione, D J Klaus, E Y Yeh, et al.
Journal of Medical Genetics|December 14, 1999
Familial gastric cancer: overview and guidelines for managementC Caldas, F Carneiro, H T Lynch, et al.
Journal of Medical Genetics|July 6, 2004
Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteriaA R Brooks-Wilson, P Kaurah, G Suriano, et al.
Nature Genetics|November 16, 2002
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndromeJ D Carpten, C M Robbins, A Villablanca, et al.
Pageof 18

Showing results (171-180 of 180) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 180 results.
Nature Genetics|June 1, 1996
Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2D W Johnson, J N Berg, M A Baldwin, et al.
American Journal of Human Genetics|May 1, 1997
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.
QJM : Monthly Journal of the Association of Physicians|September 1, 1996
Clinical studies of multiple endocrine neoplasia type 1 (MEN1)D Trump, B Farren, C Wooding, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.
Blood|June 22, 2001
The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosisS E Straus, E S Jaffe, J M Puck, et al.
Neurology|February 27, 2001
Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathyJ R Mendell, R J Barohn, M L Freimer, et al.
Human Mutation|April 29, 1998
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null allelesC J Gallione, D J Klaus, E Y Yeh, et al.
Journal of Medical Genetics|December 14, 1999
Familial gastric cancer: overview and guidelines for managementC Caldas, F Carneiro, H T Lynch, et al.
Journal of Medical Genetics|July 6, 2004
Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteriaA R Brooks-Wilson, P Kaurah, G Suriano, et al.
Nature Genetics|November 16, 2002
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndromeJ D Carpten, C M Robbins, A Villablanca, et al.
Pageof 18