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A Giedion

Showing results (31-40 of 49) with videos related to

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Helvetica Paediatrica Acta|November 1, 1978
Unusually mild course of beta-glucuronidase deficiency in two brothers (mucopolysaccharidosis VII)R Gitzelmann, U N Wiesmann, M A Spycher, et al.
American Journal of Medical Genetics|May 3, 1996
Metaphyseal peg in geroderma osteodysplasticum: a new genetic bone marker and a specific finding?G F Eich, B Steinmann, J Hodler, et al.
Helvetica Paediatrica Acta|September 1, 1982
Oto-spondylo-megaepiphyseal dysplasia (OSMED)A Giedion, M Brandner, J Lecannellier, 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.
Schweizerische Medizinische Wochenschrift|September 23, 1989
[Long-term course in congenital analgesia]M Losa, H Scheier, P Rohner, et al.
The Journal of Pediatrics|September 1, 1986
Kenny syndrome: evidence for idiopathic hypoparathyroidism in two patients and for abnormal parathyroid hormone in oneS Fanconi, J A Fischer, P Wieland, et al.
Clinical Genetics|May 1, 1976
Spondyloepiphyseal dysplasia, corneal clouding, normal intelligence and acid beta-galactosidase deficiencyJ S O'Brien, E Gugler, A Giedion, et al.
American Journal of Medical Genetics|July 23, 1998
Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: a case for "lumping"A Superti-Furga, R Tenconi, M Clementi, et al.
American Journal of Medical Genetics. Part A|November 4, 2004
Pronounced short stature in a girl with tricho-rhino-phalangeal syndrome II (TRPS II, Langer-Giedion syndrome) and growth hormone deficiencyS Riedl, A Giedion, K Schweitzer, et al.
Journal of Medical Genetics|January 1, 1991
Unknown syndrome: ischiadic hypoplasia, renal dysfunction, immunodeficiency, and a pattern of minor congenital anomaliesC Braegger, A Bottani, F Hallé, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Helvetica Paediatrica Acta|November 1, 1978
Unusually mild course of beta-glucuronidase deficiency in two brothers (mucopolysaccharidosis VII)R Gitzelmann, U N Wiesmann, M A Spycher, et al.
American Journal of Medical Genetics|May 3, 1996
Metaphyseal peg in geroderma osteodysplasticum: a new genetic bone marker and a specific finding?G F Eich, B Steinmann, J Hodler, et al.
Helvetica Paediatrica Acta|September 1, 1982
Oto-spondylo-megaepiphyseal dysplasia (OSMED)A Giedion, M Brandner, J Lecannellier, 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.
Schweizerische Medizinische Wochenschrift|September 23, 1989
[Long-term course in congenital analgesia]M Losa, H Scheier, P Rohner, et al.
The Journal of Pediatrics|September 1, 1986
Kenny syndrome: evidence for idiopathic hypoparathyroidism in two patients and for abnormal parathyroid hormone in oneS Fanconi, J A Fischer, P Wieland, et al.
Clinical Genetics|May 1, 1976
Spondyloepiphyseal dysplasia, corneal clouding, normal intelligence and acid beta-galactosidase deficiencyJ S O'Brien, E Gugler, A Giedion, et al.
American Journal of Medical Genetics|July 23, 1998
Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: a case for "lumping"A Superti-Furga, R Tenconi, M Clementi, et al.
American Journal of Medical Genetics. Part A|November 4, 2004
Pronounced short stature in a girl with tricho-rhino-phalangeal syndrome II (TRPS II, Langer-Giedion syndrome) and growth hormone deficiencyS Riedl, A Giedion, K Schweitzer, et al.
Journal of Medical Genetics|January 1, 1991
Unknown syndrome: ischiadic hypoplasia, renal dysfunction, immunodeficiency, and a pattern of minor congenital anomaliesC Braegger, A Bottani, F Hallé, et al.
Pageof 5