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U Moog

Showing results (11-20 of 46) with videos related to

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Familial Cancer|October 24, 2003
Chemotherapy resistant ovarian cancer in carriers of an hMSH2 mutation?C L Marcelis, H W van der Putten, C Tops, et al.
American Journal of Medical Genetics|July 24, 1998
Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?U Moog, E M Bleeker-Wagemakers, P Crobach, et al.
AJNR. American Journal of Neuroradiology|May 4, 2019
Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem InvolvementI Harting, S Karch, U Moog, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Oculocerebrocutaneous syndrome: a case report, a follow-up, and differential diagnostic considerationsU Moog, G Krüger, B Stengel, et al.
American Journal of Medical Genetics|October 20, 2000
Familial dup(8)(p12p21.1): mild phenotypic effect and review of partial 8p duplicationsU Moog, J J Engelen, J C Albrechts, et al.
American Journal of Medical Genetics|April 6, 2000
Duplication of chromosome region 8p23.1-->p23.3: a benign variant?J J Engelen, U Moog, J L Evers, et al.
Clinical Genetics|May 1, 1996
Marker chromosome identification by micro-FISHJ J Engelen, W J Loots, P C Motoh, et al.
Journal of Medical Genetics|November 2, 1999
Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?U Moog, P Maroteaux, C T Schrander-Stumpel, et al.
Clinical Genetics|August 29, 2013
PIK3R1 mutations in SHORT syndromeC Schroeder, A Riess, M Bonin, et al.
American Journal of Medical Genetics|September 24, 1999
Epidermolysis bullosa simplex with mottled pigmentation: clinical aspects and confirmation of the P24L mutation in the KRT5 gene in further patientsU Moog, C E de Die-Smulders, H Scheffer, et al.
Pageof 5

Showing results (11-20 of 46) with videos related to

Sort By:
Pageof 5
Familial Cancer|October 24, 2003
Chemotherapy resistant ovarian cancer in carriers of an hMSH2 mutation?C L Marcelis, H W van der Putten, C Tops, et al.
American Journal of Medical Genetics|July 24, 1998
Sibs with Axenfeld-Rieger anomaly, hydrocephalus, and leptomeningeal calcifications: a new autosomal recessive syndrome?U Moog, E M Bleeker-Wagemakers, P Crobach, et al.
AJNR. American Journal of Neuroradiology|May 4, 2019
Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem InvolvementI Harting, S Karch, U Moog, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Oculocerebrocutaneous syndrome: a case report, a follow-up, and differential diagnostic considerationsU Moog, G Krüger, B Stengel, et al.
American Journal of Medical Genetics|October 20, 2000
Familial dup(8)(p12p21.1): mild phenotypic effect and review of partial 8p duplicationsU Moog, J J Engelen, J C Albrechts, et al.
American Journal of Medical Genetics|April 6, 2000
Duplication of chromosome region 8p23.1-->p23.3: a benign variant?J J Engelen, U Moog, J L Evers, et al.
Clinical Genetics|May 1, 1996
Marker chromosome identification by micro-FISHJ J Engelen, W J Loots, P C Motoh, et al.
Journal of Medical Genetics|November 2, 1999
Two sibs with an unusual pattern of skeletal malformations resembling osteogenesis imperfecta: a new type of skeletal dysplasia?U Moog, P Maroteaux, C T Schrander-Stumpel, et al.
Clinical Genetics|August 29, 2013
PIK3R1 mutations in SHORT syndromeC Schroeder, A Riess, M Bonin, et al.
American Journal of Medical Genetics|September 24, 1999
Epidermolysis bullosa simplex with mottled pigmentation: clinical aspects and confirmation of the P24L mutation in the KRT5 gene in further patientsU Moog, C E de Die-Smulders, H Scheffer, et al.
Pageof 5