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American Journal of Medical Genetics
|
March 4, 2000
Cri du chat syndrome: changing phenotype in older patients
G J Van Buggenhout, E Pijkels, M Holvoet, et al.
Cell Cycle (Georgetown, Tex.)
|
January 19, 2006
GW bodies, microRNAs and the cell cycle
Shangli Lian, Andrew Jakymiw, Theophany Eystathioy, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology
|
June 20, 2019
Current and future expectations of mifepristone treatment in early pregnancy failure: a survey among Dutch gynaecologists
Joyce van den Berg, Charlotte C Hamel, Sjors F Coppus, et al.
Endocrine Research
|
November 1, 1996
Production and metabolism of serotonin (5-HT) by the human adrenal gland
H Lefebvre, P Compagnon, V Contesse, et al.
EMBO Reports
|
August 15, 2006
Formation of GW bodies is a consequence of microRNA genesis
Kaleb M Pauley, Theophany Eystathioy, Andrew Jakymiw, et al.
Arthritis Research
|
July 11, 2002
Fragmentation of Golgi complex and Golgi autoantigens during apoptosis and necrosis
Kazuhisa Nozawa, Carlos A Casiano, John C Hamel, et al.
American Journal of Medical Genetics. Part A
|
August 21, 2007
Ehlers-Danlos syndrome due to tenascin-X deficiency: muscle weakness and contractures support overlap with collagen VI myopathies
N C Voermans, G J Jenniskens, B C Hamel, et al.
American Journal of Medical Genetics
|
July 15, 1994
Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies
B C Hamel, E C Mariman, S E van Beersum, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery
|
September 22, 2007
Comparison of 1% and 3% polidocanol foam in ultrasound guided sclerotherapy of the great saphenous vein: a randomised, double-blind trial with 2 year-follow-up. "The 3/1 Study"
C Hamel-Desnos, P Ouvry, J-P Benigni, et al.
Oxford Medical Case Reports
|
July 24, 2018
Camurati-Engelmann disease: a case report from sub-Saharan Africa
Amos O Mwasamwaja, Elifuraha W Mkwizu, Elichilia R Shao, et al.
Page
of 30
Search research articles
Search
Showing results (141-150 of 291) with videos related to
Sort By:
Page
of 30
American Journal of Medical Genetics
|
March 4, 2000
Cri du chat syndrome: changing phenotype in older patients
G J Van Buggenhout, E Pijkels, M Holvoet, et al.
Cell Cycle (Georgetown, Tex.)
|
January 19, 2006
GW bodies, microRNAs and the cell cycle
Shangli Lian, Andrew Jakymiw, Theophany Eystathioy, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology
|
June 20, 2019
Current and future expectations of mifepristone treatment in early pregnancy failure: a survey among Dutch gynaecologists
Joyce van den Berg, Charlotte C Hamel, Sjors F Coppus, et al.
Endocrine Research
|
November 1, 1996
Production and metabolism of serotonin (5-HT) by the human adrenal gland
H Lefebvre, P Compagnon, V Contesse, et al.
EMBO Reports
|
August 15, 2006
Formation of GW bodies is a consequence of microRNA genesis
Kaleb M Pauley, Theophany Eystathioy, Andrew Jakymiw, et al.
Arthritis Research
|
July 11, 2002
Fragmentation of Golgi complex and Golgi autoantigens during apoptosis and necrosis
Kazuhisa Nozawa, Carlos A Casiano, John C Hamel, et al.
American Journal of Medical Genetics. Part A
|
August 21, 2007
Ehlers-Danlos syndrome due to tenascin-X deficiency: muscle weakness and contractures support overlap with collagen VI myopathies
N C Voermans, G J Jenniskens, B C Hamel, et al.
American Journal of Medical Genetics
|
July 15, 1994
Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies
B C Hamel, E C Mariman, S E van Beersum, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery
|
September 22, 2007
Comparison of 1% and 3% polidocanol foam in ultrasound guided sclerotherapy of the great saphenous vein: a randomised, double-blind trial with 2 year-follow-up. "The 3/1 Study"
C Hamel-Desnos, P Ouvry, J-P Benigni, et al.
Oxford Medical Case Reports
|
July 24, 2018
Camurati-Engelmann disease: a case report from sub-Saharan Africa
Amos O Mwasamwaja, Elifuraha W Mkwizu, Elichilia R Shao, et al.
Page
of 30