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Clinical Genetics
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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 stature
M 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 leukodystrophy
S Spranger, M Spranger, K Kirchhof, et al.
American Journal of Medical Genetics
|
July 3, 1995
Two sisters with Escobar syndrome
S Spranger, M Spranger, H M Meinck, et al.
European Neurology
|
April 15, 1999
Familial hemiplegic migraine with cerebellar ataxia and paroxysmal psychosis
M 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 retardation
M 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 involvement
S Spranger, M Weber, J Tröger, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 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 stature
M 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 leukodystrophy
S Spranger, M Spranger, K Kirchhof, et al.
American Journal of Medical Genetics
|
July 3, 1995
Two sisters with Escobar syndrome
S Spranger, M Spranger, H M Meinck, et al.
European Neurology
|
April 15, 1999
Familial hemiplegic migraine with cerebellar ataxia and paroxysmal psychosis
M 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 retardation
M 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 involvement
S Spranger, M Weber, J Tröger, et al.
Page
of 4