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J Spranger

Showing results (121-130 of 247) with videos related to

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Skeletal Radiology|January 1, 1982
Wormian bones in osteogenesis imperfecta and other disordersB Cremin, H Goodman, J Spranger, et al.
Journal of Neurology|August 4, 1975
[The occurrence of diabetes mellitus, diabetes insipidus, optic atrophy and neurogenic deafness in one patient (author's transl)]K Foerster, J Spranger, J Beyer, et al.
American Journal of Medical Genetics|June 19, 1998
Classification of limb defectsC Stoll, D Duboule, L B Holmes, et al.
Diabetes|September 1, 1997
Growth factor alterations in advanced diabetic retinopathy: a possible role of blood retina barrier breakdownA Pfeiffer, J Spranger, R Meyer-Schwickerath, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|November 21, 1987
Morquio's disease type B (beta-galactosidase deficiency) in three siblingsM Beck, E M Petersen, J Spranger, et al.
Pediatric Radiology|December 4, 1978
Two peculiar types of enchondromatosisJ Spranger, H Kemperdieck, H Bakowski, et al.
Lancet (London, England)|November 2, 1974
Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiencyJ Spranger, J Gehler, J F O'Brien, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1996
Neurology of adult alpha-mannosidosisS Niemann, M Beck, G Seidel, et al.
American Journal of Medical Genetics|May 3, 1996
An unknown spondylo-meta-epiphyseal dysplasia in sibs with extreme short statureH Menger, S Mundlos, K Becker, et al.
American Journal of Medical Genetics|October 1, 1993
Cerebral malformation, seizures, hypertrichosis, distinct face, claw hands, and overlapping fingers in sibs of both sexesF M Müller, G M Barth, H Menger, et al.
Pageof 25

Showing results (121-130 of 247) with videos related to

Sort By:
Pageof 25
Skeletal Radiology|January 1, 1982
Wormian bones in osteogenesis imperfecta and other disordersB Cremin, H Goodman, J Spranger, et al.
Journal of Neurology|August 4, 1975
[The occurrence of diabetes mellitus, diabetes insipidus, optic atrophy and neurogenic deafness in one patient (author's transl)]K Foerster, J Spranger, J Beyer, et al.
American Journal of Medical Genetics|June 19, 1998
Classification of limb defectsC Stoll, D Duboule, L B Holmes, et al.
Diabetes|September 1, 1997
Growth factor alterations in advanced diabetic retinopathy: a possible role of blood retina barrier breakdownA Pfeiffer, J Spranger, R Meyer-Schwickerath, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|November 21, 1987
Morquio's disease type B (beta-galactosidase deficiency) in three siblingsM Beck, E M Petersen, J Spranger, et al.
Pediatric Radiology|December 4, 1978
Two peculiar types of enchondromatosisJ Spranger, H Kemperdieck, H Bakowski, et al.
Lancet (London, England)|November 2, 1974
Letter: Chondroitinsulphaturia with alpha-L-iduronidase deficiencyJ Spranger, J Gehler, J F O'Brien, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1996
Neurology of adult alpha-mannosidosisS Niemann, M Beck, G Seidel, et al.
American Journal of Medical Genetics|May 3, 1996
An unknown spondylo-meta-epiphyseal dysplasia in sibs with extreme short statureH Menger, S Mundlos, K Becker, et al.
American Journal of Medical Genetics|October 1, 1993
Cerebral malformation, seizures, hypertrichosis, distinct face, claw hands, and overlapping fingers in sibs of both sexesF M Müller, G M Barth, H Menger, et al.
Pageof 25