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Showing results (41-50 of 61) with videos related to

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Thrombosis and Haemostasis|February 11, 2000
The half-life of infused factor VIII is shorter in hemophiliac patients with blood group O than in those with blood group AA J Vlot, E P Mauser-Bunschoten, A G Zarkova, et al.
Neuromuscular Disorders : NMD|February 17, 2015
Non-coding VMA21 deletions cause X-linked myopathy with excessive autophagyA Ruggieri, N Ramachandran, P Wang, et al.
British Journal of Cancer|January 22, 2004
Communication and information-giving in high-risk breast cancer consultations: influence on patient outcomesE A Lobb, P N Butow, A Barratt, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Effect and side-effects of alpha interferon treatment in haemophilia patients with chronic hepatitis CE P Mauser-Bunschoten, D Bresters, H W Reesink, et al.
American Journal of Human Genetics|October 23, 1997
Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 geneJ R Sampson, M M Maheshwar, R Aspinwall, et al.
Journal of Medical Genetics|May 16, 2009
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotypeG Spurlock, E Bennett, N Chuzhanova, et al.
Cytogenetic and Genome Research|April 18, 2009
A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technologyB A Talseth-Palmer, N A Bowden, C Meldrum, et al.
Biomaterials|September 27, 2002
Bone growth in biomimetic apatite coated porous Polyactive 1000PEGT70PBT30 implantsC Du, G J Meijer, C van de Valk, et al.
The Journal of Pathology|October 24, 2007
Chronic colitis due to an epithelial barrier defect: the role of kindlin-1 isoformsJ S Kern, C Herz, E Haan, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa-Kuroki) syndromeS M White, E M Thompson, A Kidd, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Thrombosis and Haemostasis|February 11, 2000
The half-life of infused factor VIII is shorter in hemophiliac patients with blood group O than in those with blood group AA J Vlot, E P Mauser-Bunschoten, A G Zarkova, et al.
Neuromuscular Disorders : NMD|February 17, 2015
Non-coding VMA21 deletions cause X-linked myopathy with excessive autophagyA Ruggieri, N Ramachandran, P Wang, et al.
British Journal of Cancer|January 22, 2004
Communication and information-giving in high-risk breast cancer consultations: influence on patient outcomesE A Lobb, P N Butow, A Barratt, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 24, 2016
Effect and side-effects of alpha interferon treatment in haemophilia patients with chronic hepatitis CE P Mauser-Bunschoten, D Bresters, H W Reesink, et al.
American Journal of Human Genetics|October 23, 1997
Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 geneJ R Sampson, M M Maheshwar, R Aspinwall, et al.
Journal of Medical Genetics|May 16, 2009
SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotypeG Spurlock, E Bennett, N Chuzhanova, et al.
Cytogenetic and Genome Research|April 18, 2009
A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technologyB A Talseth-Palmer, N A Bowden, C Meldrum, et al.
Biomaterials|September 27, 2002
Bone growth in biomimetic apatite coated porous Polyactive 1000PEGT70PBT30 implantsC Du, G J Meijer, C van de Valk, et al.
The Journal of Pathology|October 24, 2007
Chronic colitis due to an epithelial barrier defect: the role of kindlin-1 isoformsJ S Kern, C Herz, E Haan, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa-Kuroki) syndromeS M White, E M Thompson, A Kidd, et al.
Pageof 7