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C Hamel

Showing results (91-100 of 291) with videos related to

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Southern Medical Journal|May 1, 1982
Complete heart block caused by hemorrhage into the atrioventricular conduction pathwayM A Alpert, J D Dix, P C Hamel, et al.
American Journal of Medical Genetics|March 1, 1990
Acrocallosal syndromeH J Hendriks, H G Brunner, T A Haagen, et al.
American Journal of Human Genetics|October 1, 1996
Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growthL A Pérez Jurado, R Peoples, P Kaplan, et al.
Journal of Neurosurgery|March 1, 1987
Treatment of bilateral spontaneous dural carotid-cavernous fistulas by coils and sclerotherapy. Case reportP Courtheoux, D Labbe, C Hamel, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Zimmermann-Laband syndrome in a patient with severe mental retardationG J Van Buggenhout, H G Brunner, J C Trommelen, et al.
Nederlands Tijdschrift Voor Geneeskunde|July 14, 2016
[Thoracic endometriosis with aspecific manifestation]C C Hamel, J H de Kruif, J P Jansen, et al.
Ophthalmic Genetics|October 16, 1999
Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998999ins4C Bareil, C Hamel, N Pallarès-Ruiz, et al.
American Journal of Medical Genetics|May 15, 1994
Spondylocarpotarsal synostosis syndrome (with or without unilateral unsegmented bar)L O Langer, R J Gorlin, D Donnai, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|November 1, 1990
[Value of a velocimetric study of the uterine arteries in retroplacental hematoma. 3 case reports]C Hamel-Desnos, P Philippart, P Desnos, et al.
European Journal of Human Genetics : EJHG|July 6, 2000
A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndromeL Tranebjaerg, B C Hamel, F J Gabreels, et al.
Pageof 30

Showing results (91-100 of 291) with videos related to

Sort By:
Pageof 30
Southern Medical Journal|May 1, 1982
Complete heart block caused by hemorrhage into the atrioventricular conduction pathwayM A Alpert, J D Dix, P C Hamel, et al.
American Journal of Medical Genetics|March 1, 1990
Acrocallosal syndromeH J Hendriks, H G Brunner, T A Haagen, et al.
American Journal of Human Genetics|October 1, 1996
Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growthL A Pérez Jurado, R Peoples, P Kaplan, et al.
Journal of Neurosurgery|March 1, 1987
Treatment of bilateral spontaneous dural carotid-cavernous fistulas by coils and sclerotherapy. Case reportP Courtheoux, D Labbe, C Hamel, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Zimmermann-Laband syndrome in a patient with severe mental retardationG J Van Buggenhout, H G Brunner, J C Trommelen, et al.
Nederlands Tijdschrift Voor Geneeskunde|July 14, 2016
[Thoracic endometriosis with aspecific manifestation]C C Hamel, J H de Kruif, J P Jansen, et al.
Ophthalmic Genetics|October 16, 1999
Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998999ins4C Bareil, C Hamel, N Pallarès-Ruiz, et al.
American Journal of Medical Genetics|May 15, 1994
Spondylocarpotarsal synostosis syndrome (with or without unilateral unsegmented bar)L O Langer, R J Gorlin, D Donnai, et al.
Revue Francaise De Gynecologie Et D'Obstetrique|November 1, 1990
[Value of a velocimetric study of the uterine arteries in retroplacental hematoma. 3 case reports]C Hamel-Desnos, P Philippart, P Desnos, et al.
European Journal of Human Genetics : EJHG|July 6, 2000
A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndromeL Tranebjaerg, B C Hamel, F J Gabreels, et al.
Pageof 30