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J W Spranger

Showing results (31-40 of 46) with videos related to

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The Journal of Pediatrics|September 1, 1971
I-cell disease: a clinical pictureJ G Leroy, J W Spranger, M Feingold, et al.
Birth Defects Original Article Series|January 1, 1974
Pathology of chondrodysplasia punctata rhizomelic typeC Viseskul, J M Opitz, J W Spranger, et al.
American Journal of Medical Genetics|January 1, 1980
Cerebroarthrodigital syndrome: a newly recognized formal genesis syndrome in three patients with apparent arthromyodysplasia and sacral agenesis, brain malformation and digital hypoplasiaJ W Spranger, A Schinzel, T Myers, et al.
Helvetica Paediatrica Acta|October 1, 1970
Mucopolysaccharidosis VI (Maroteaux-Lamy's disease)J W Spranger, F Koch, V A McKusick, et al.
Lancet (London, England)|July 10, 1971
Geleophysic dwarfism--a "focal" mucopolysaccharidosis?J W Spranger, E F Gilbert, G A Tuffli, et al.
American Journal of Medical Genetics|December 1, 1985
An autosomal dominant syndrome of short stature with mesomelic shortness of limbs, abnormal carpal and tarsal bones, hypoplastic middle phalanges, and bipartite calcaneiW R Osebold, D J Remondini, E L Lester, et al.
European Journal of Pediatrics|January 2, 1976
Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of Zellweger: comparative pathologyK W Gilchrist, E F Gilbert, S Goldfarb, et al.
European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.
Birth Defects Original Article Series|January 1, 1974
The W syndrome. Studies of malformation syndromes of man XXVIIIP D Pallister, J Herrmann, J W Spranger, et al.
American Journal of Medical Genetics|December 8, 1998
Previously undescribed syndrome of spondylometaphyseal dysplasia, osteocartilaginous metaplasia of long bones, and progressive osteolysis of distal phalangesW R Osebold, A K Poznanski, J M Opitz, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
The Journal of Pediatrics|September 1, 1971
I-cell disease: a clinical pictureJ G Leroy, J W Spranger, M Feingold, et al.
Birth Defects Original Article Series|January 1, 1974
Pathology of chondrodysplasia punctata rhizomelic typeC Viseskul, J M Opitz, J W Spranger, et al.
American Journal of Medical Genetics|January 1, 1980
Cerebroarthrodigital syndrome: a newly recognized formal genesis syndrome in three patients with apparent arthromyodysplasia and sacral agenesis, brain malformation and digital hypoplasiaJ W Spranger, A Schinzel, T Myers, et al.
Helvetica Paediatrica Acta|October 1, 1970
Mucopolysaccharidosis VI (Maroteaux-Lamy's disease)J W Spranger, F Koch, V A McKusick, et al.
Lancet (London, England)|July 10, 1971
Geleophysic dwarfism--a "focal" mucopolysaccharidosis?J W Spranger, E F Gilbert, G A Tuffli, et al.
American Journal of Medical Genetics|December 1, 1985
An autosomal dominant syndrome of short stature with mesomelic shortness of limbs, abnormal carpal and tarsal bones, hypoplastic middle phalanges, and bipartite calcaneiW R Osebold, D J Remondini, E L Lester, et al.
European Journal of Pediatrics|January 2, 1976
Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of Zellweger: comparative pathologyK W Gilchrist, E F Gilbert, S Goldfarb, et al.
European Journal of Pediatrics|September 1, 1976
Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infantsE F Gilbert, J M Opitz, J W Spranger, et al.
Birth Defects Original Article Series|January 1, 1974
The W syndrome. Studies of malformation syndromes of man XXVIIIP D Pallister, J Herrmann, J W Spranger, et al.
American Journal of Medical Genetics|December 8, 1998
Previously undescribed syndrome of spondylometaphyseal dysplasia, osteocartilaginous metaplasia of long bones, and progressive osteolysis of distal phalangesW R Osebold, A K Poznanski, J M Opitz, et al.
Pageof 5