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S Spranger

Showing results (11-20 of 34) with videos related to

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Muscle & Nerve|July 1, 1996
Köbberling-Dunnigan syndrome: a rare cause of generalized muscular hypertrophyS Wildermuth, S Spranger, M Spranger, et al.
American Journal of Medical Genetics|June 27, 2000
Interstitial deletion of 5q33.3q35.1 in a girl with mild mental retardationS Spranger, B Rommel, A Jauch, et al.
The Journal of Bone and Joint Surgery. American Volume|March 12, 1999
Ehlers-Danlos syndrome type VII: clinical features and molecular defectsC Giunta, A Superti-Furga, S Spranger, et al.
Clinical Genetics|May 1, 1997
Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal heightS Spranger, S Kirsch, A Mertz, et al.
Journal of Medical Genetics|April 1, 1997
Proximal and distal spinal muscular atrophy in one family: molecular genetic studies provide further evidence for the non-allelic origin of both diseasesS Spranger, S Rudnik-Schöneborn, M Spranger, et al.
American Journal of Medical Genetics|September 5, 1997
Barraquer-Simons syndrome (with sensorineural deafness): a contribution to the differential diagnosis of lipodystrophy syndromesS Spranger, M Spranger, A J Tasman, et al.
Clinical Genetics|January 4, 2012
Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome featuresT Eggermann, S Spengler, M Begemann, et al.
European Journal of Pediatrics|September 1, 1996
Case report. Microcephalic osteodysplastic primordial dwarfism type II: a child with unusual symptoms and clinical courseS Spranger, G Tariverdian, F K Albert, et al.
Journal of Medical Genetics|January 16, 1998
Muscular involvement in the Holt-Oram syndromeS Spranger, H Ulmer, J Tröger, et al.
Annales De Genetique|May 4, 2001
Origin of uniparental disomy 6: presentation of a new case and review on the literatureT Eggermann, W Marg, S Mergenthaler, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Muscle & Nerve|July 1, 1996
Köbberling-Dunnigan syndrome: a rare cause of generalized muscular hypertrophyS Wildermuth, S Spranger, M Spranger, et al.
American Journal of Medical Genetics|June 27, 2000
Interstitial deletion of 5q33.3q35.1 in a girl with mild mental retardationS Spranger, B Rommel, A Jauch, et al.
The Journal of Bone and Joint Surgery. American Volume|March 12, 1999
Ehlers-Danlos syndrome type VII: clinical features and molecular defectsC Giunta, A Superti-Furga, S Spranger, et al.
Clinical Genetics|May 1, 1997
Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal heightS Spranger, S Kirsch, A Mertz, et al.
Journal of Medical Genetics|April 1, 1997
Proximal and distal spinal muscular atrophy in one family: molecular genetic studies provide further evidence for the non-allelic origin of both diseasesS Spranger, S Rudnik-Schöneborn, M Spranger, et al.
American Journal of Medical Genetics|September 5, 1997
Barraquer-Simons syndrome (with sensorineural deafness): a contribution to the differential diagnosis of lipodystrophy syndromesS Spranger, M Spranger, A J Tasman, et al.
Clinical Genetics|January 4, 2012
Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome featuresT Eggermann, S Spengler, M Begemann, et al.
European Journal of Pediatrics|September 1, 1996
Case report. Microcephalic osteodysplastic primordial dwarfism type II: a child with unusual symptoms and clinical courseS Spranger, G Tariverdian, F K Albert, et al.
Journal of Medical Genetics|January 16, 1998
Muscular involvement in the Holt-Oram syndromeS Spranger, H Ulmer, J Tröger, et al.
Annales De Genetique|May 4, 2001
Origin of uniparental disomy 6: presentation of a new case and review on the literatureT Eggermann, W Marg, S Mergenthaler, et al.
Pageof 4