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N Van Regemorter

Showing results (31-40 of 71) with videos related to

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Journal of Neurology|January 1, 1979
Charcot-Marie-Tooth disease associated with retinal pigment dystrophy and protanopia. Neurological, ophthalmological and genetic study of a familyP Khoubesserian, N van Regemorter, O Ohrn-Degueldre, et al.
Acta Oto-Rhino-Laryngologica Belgica|January 1, 1985
[Etiological evaluation of deafness in children]H B Szliwowski, M Courtoy, R Bourgeois, et al.
Pediatric Neurology|January 8, 1999
Gray matter heterotopia and acute necrotizing encephalopathy in trichothiodystrophyC L Wetzburger, N Van Regemorter, H B Szliwowski, et al.
Revue Medicale De Bruxelles|October 1, 1984
[Prenatal diagnosis of digestive system malformations using echography]N Elkhazen, J Dodion, E Vamos, et al.
Prenatal Diagnosis|July 21, 2005
Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound?M Staebler, C Donner, N Van Regemorter, et al.
European Journal of Pediatrics|October 1, 1983
Partial trisomy 3p in two siblings: clinical and pathological findingsN Van Regemorter, E Vamos, Y Gillerot, et al.
American Journal of Medical Genetics|April 1, 1984
Lethal multiple pterygium syndromeN Van Regemorter, P Wilkin, Y Englert, et al.
Prenatal Diagnosis|January 1, 1985
A case of partial sirenomelia and possible vitamin A teratogenesisE Von Lennep, N El Khazen, G De Pierreux, et al.
Annales De Genetique|January 1, 1991
Association of the Hind III polymorphism with the androgen receptor gene in partial androgen insensitivity syndromeJ M Lobaccaro, C Belon, R Ruiz-Pacheco, et al.
American Journal of Medical Genetics|March 1, 1986
Lethal osteopetrosis with multiple fractures in uteroN el Khazen, D Faverly, E Vamos, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
Journal of Neurology|January 1, 1979
Charcot-Marie-Tooth disease associated with retinal pigment dystrophy and protanopia. Neurological, ophthalmological and genetic study of a familyP Khoubesserian, N van Regemorter, O Ohrn-Degueldre, et al.
Acta Oto-Rhino-Laryngologica Belgica|January 1, 1985
[Etiological evaluation of deafness in children]H B Szliwowski, M Courtoy, R Bourgeois, et al.
Pediatric Neurology|January 8, 1999
Gray matter heterotopia and acute necrotizing encephalopathy in trichothiodystrophyC L Wetzburger, N Van Regemorter, H B Szliwowski, et al.
Revue Medicale De Bruxelles|October 1, 1984
[Prenatal diagnosis of digestive system malformations using echography]N Elkhazen, J Dodion, E Vamos, et al.
Prenatal Diagnosis|July 21, 2005
Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound?M Staebler, C Donner, N Van Regemorter, et al.
European Journal of Pediatrics|October 1, 1983
Partial trisomy 3p in two siblings: clinical and pathological findingsN Van Regemorter, E Vamos, Y Gillerot, et al.
American Journal of Medical Genetics|April 1, 1984
Lethal multiple pterygium syndromeN Van Regemorter, P Wilkin, Y Englert, et al.
Prenatal Diagnosis|January 1, 1985
A case of partial sirenomelia and possible vitamin A teratogenesisE Von Lennep, N El Khazen, G De Pierreux, et al.
Annales De Genetique|January 1, 1991
Association of the Hind III polymorphism with the androgen receptor gene in partial androgen insensitivity syndromeJ M Lobaccaro, C Belon, R Ruiz-Pacheco, et al.
American Journal of Medical Genetics|March 1, 1986
Lethal osteopetrosis with multiple fractures in uteroN el Khazen, D Faverly, E Vamos, et al.
Pageof 8