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S Spranger

Showing results (1-10 of 34) with videos related to

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Clinical Genetics|April 1, 1995
Symptomatic heterozygosity in the Ellis-van Creveld syndrome?S Spranger, G Tariverdian
Journal of Craniofacial Genetics and Developmental Biology|April 26, 2001
Distinctive pitted enamel hypoplasia and short statureM J Koch, S Spranger, M Bettendorf
Der Nervenarzt|March 31, 1999
[Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion]M Spranger, B Janssen, D Rating, et al.
American Journal of Medical Genetics|December 11, 1996
Ehlers-Danlos syndrome type VIII and leukodystrophyS Spranger, M Spranger, K Kirchhof, et al.
American Journal of Medical Genetics|July 3, 1995
Two sisters with Escobar syndromeS Spranger, M Spranger, H M Meinck, et al.
European Neurology|April 15, 1999
Familial hemiplegic migraine with cerebellar ataxia and paroxysmal psychosisM Spranger, S Spranger, S Schwab, et al.
American Journal of Medical Genetics. Part A|August 19, 2003
Congenital generalized lipodystrophy, mental retardation, deafness, short stature, and slender bones: a newly recognized syndrome?A Rajab, M Khaburi, S Spranger, et al.
Archives of Neurology|March 1, 1997
Myotonic dystrophy. The role of large triplet repeat length in the development of mental retardationM Spranger, S Spranger, M Tischendorf, et al.
Clinical Genetics|October 1, 1996
Three familial cases presenting with an immobile spine. Rigid spine or Emery-Dreifuss syndrome?M Spranger, S Spranger, J Ziegan, et al.
American Journal of Medical Genetics|May 3, 1996
Bilateral radial deficiency with lower limb involvementS Spranger, M Weber, J Tröger, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Clinical Genetics|April 1, 1995
Symptomatic heterozygosity in the Ellis-van Creveld syndrome?S Spranger, G Tariverdian
Journal of Craniofacial Genetics and Developmental Biology|April 26, 2001
Distinctive pitted enamel hypoplasia and short statureM J Koch, S Spranger, M Bettendorf
Der Nervenarzt|March 31, 1999
[Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion]M Spranger, B Janssen, D Rating, et al.
American Journal of Medical Genetics|December 11, 1996
Ehlers-Danlos syndrome type VIII and leukodystrophyS Spranger, M Spranger, K Kirchhof, et al.
American Journal of Medical Genetics|July 3, 1995
Two sisters with Escobar syndromeS Spranger, M Spranger, H M Meinck, et al.
European Neurology|April 15, 1999
Familial hemiplegic migraine with cerebellar ataxia and paroxysmal psychosisM Spranger, S Spranger, S Schwab, et al.
American Journal of Medical Genetics. Part A|August 19, 2003
Congenital generalized lipodystrophy, mental retardation, deafness, short stature, and slender bones: a newly recognized syndrome?A Rajab, M Khaburi, S Spranger, et al.
Archives of Neurology|March 1, 1997
Myotonic dystrophy. The role of large triplet repeat length in the development of mental retardationM Spranger, S Spranger, M Tischendorf, et al.
Clinical Genetics|October 1, 1996
Three familial cases presenting with an immobile spine. Rigid spine or Emery-Dreifuss syndrome?M Spranger, S Spranger, J Ziegan, et al.
American Journal of Medical Genetics|May 3, 1996
Bilateral radial deficiency with lower limb involvementS Spranger, M Weber, J Tröger, et al.
Pageof 4