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Neurogenetics
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October 20, 2005
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis
K Poirier, D Lacombe, B Gilbert-Dussardier, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 30, 2010
Progressive osseous heteroplasia: a model for the imprinting effects of GNAS inactivating mutations in humans
M Lebrun, N Richard, G Abeguilé, et al.
Clinical Pharmacology and Therapeutics
|
September 20, 2016
PIPELINEs: Creating Comparable Clinical Knowledge Efficiently by Linking Trial Platforms
M R Trusheim, A A Shrier, Z Antonijevic, et al.
Journal of Medical Genetics
|
April 16, 1999
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome
L Villard, M C Bonino, F Abidi, et al.
Clinical Genetics
|
December 1, 1996
Increased paternal age in CHARGE association
A L Tellier, S Lyonnet, V Cormier-Daire, et al.
Journal of Medical Genetics
|
November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experience
B Keren, A Hadchouel, S Saba, et al.
Clinical Genetics
|
June 22, 2018
IL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differences
E Brischoux-Boucher, A Trimouille, G Baujat, et al.
Journal of Medical Genetics
|
May 4, 2004
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome
L Pinson, J Augé, S Audollent, et al.
European Journal of Cancer (Oxford, England : 1990)
|
December 23, 2008
New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1)
E A Eisenhauer, P Therasse, J Bogaerts, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 15, 2000
Oxaliplatin or paclitaxel in patients with platinum-pretreated advanced ovarian cancer: A randomized phase II study of the European Organization for Research and Treatment of Cancer Gynecology Group
M J Piccart, J A Green, A J Lacave, et al.
Page
of 23
Search research articles
Search
Showing results (181-190 of 225) with videos related to
Sort By:
Page
of 23
Neurogenetics
|
October 20, 2005
Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis
K Poirier, D Lacombe, B Gilbert-Dussardier, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 30, 2010
Progressive osseous heteroplasia: a model for the imprinting effects of GNAS inactivating mutations in humans
M Lebrun, N Richard, G Abeguilé, et al.
Clinical Pharmacology and Therapeutics
|
September 20, 2016
PIPELINEs: Creating Comparable Clinical Knowledge Efficiently by Linking Trial Platforms
M R Trusheim, A A Shrier, Z Antonijevic, et al.
Journal of Medical Genetics
|
April 16, 1999
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome
L Villard, M C Bonino, F Abidi, et al.
Clinical Genetics
|
December 1, 1996
Increased paternal age in CHARGE association
A L Tellier, S Lyonnet, V Cormier-Daire, et al.
Journal of Medical Genetics
|
November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experience
B Keren, A Hadchouel, S Saba, et al.
Clinical Genetics
|
June 22, 2018
IL11RA-related Crouzon-like autosomal recessive craniosynostosis in 10 new patients: Resemblances and differences
E Brischoux-Boucher, A Trimouille, G Baujat, et al.
Journal of Medical Genetics
|
May 4, 2004
Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome
L Pinson, J Augé, S Audollent, et al.
European Journal of Cancer (Oxford, England : 1990)
|
December 23, 2008
New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1)
E A Eisenhauer, P Therasse, J Bogaerts, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
March 15, 2000
Oxaliplatin or paclitaxel in patients with platinum-pretreated advanced ovarian cancer: A randomized phase II study of the European Organization for Research and Treatment of Cancer Gynecology Group
M J Piccart, J A Green, A J Lacave, et al.
Page
of 23