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A GIEDION

Showing results (11-20 of 33) with videos related to

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Helvetica Paediatrica Acta|January 1, 1976
The radiological diagnosis of the fetal-face (= Robinow) syndrome (mesomelic dwarfism and small genitalia). Report of 3 casesA Giedion, G F Battaglia, F Bellini, et al.
Journal of Pediatric Surgery|March 1, 1987
Deleterious consequences of gastroesophageal reflux in cleft larynx surgeryE Hof, J Hirsig, A Giedion, et al.
AJR. American Journal of Roentgenology|July 1, 1977
Neonatal mucolipidosis II (I-cell disease): clinical and radiologic features in three casesH B Patriquin, P Kaplan, H P Kind, et al.
Skeletal Radiology|January 1, 1991
Case report 693: Schneckenbecken dysplasiaA Giedion, K Biedermann, J Briner, et al.
Prenatal Diagnosis|February 1, 1989
Prenatal diagnosis of Schwartz-Jampel syndrome with early manifestationU A Hunziker, G Savoldelli, E Boltshauser, et al.
Clinical Genetics|April 10, 2002
RMRP gene sequence analysis confirms a cartilage-hair hypoplasia variant with only skeletal manifestations and reveals a high density of single-nucleotide polymorphismsL Bonafé, K Schmitt, G Eich, et al.
Radiology|June 1, 1977
The pattern of shortening of the bones of the hand in PHP and PPHP--A comparison with brachydactyly E, Turner Syndrome, and acrodysostosisA K Poznanski, E A Werder, A Giedion, et al.
American Journal of Medical Genetics|October 1, 1993
Angel-shaped phalango-epiphyseal dysplasia (ASPED): identification of a new genetic bone markerA Giedion, A Prader, C Fliegel, et al.
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.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Helvetica Paediatrica Acta|January 1, 1976
The radiological diagnosis of the fetal-face (= Robinow) syndrome (mesomelic dwarfism and small genitalia). Report of 3 casesA Giedion, G F Battaglia, F Bellini, et al.
Journal of Pediatric Surgery|March 1, 1987
Deleterious consequences of gastroesophageal reflux in cleft larynx surgeryE Hof, J Hirsig, A Giedion, et al.
AJR. American Journal of Roentgenology|July 1, 1977
Neonatal mucolipidosis II (I-cell disease): clinical and radiologic features in three casesH B Patriquin, P Kaplan, H P Kind, et al.
Skeletal Radiology|January 1, 1991
Case report 693: Schneckenbecken dysplasiaA Giedion, K Biedermann, J Briner, et al.
Prenatal Diagnosis|February 1, 1989
Prenatal diagnosis of Schwartz-Jampel syndrome with early manifestationU A Hunziker, G Savoldelli, E Boltshauser, et al.
Clinical Genetics|April 10, 2002
RMRP gene sequence analysis confirms a cartilage-hair hypoplasia variant with only skeletal manifestations and reveals a high density of single-nucleotide polymorphismsL Bonafé, K Schmitt, G Eich, et al.
Radiology|June 1, 1977
The pattern of shortening of the bones of the hand in PHP and PPHP--A comparison with brachydactyly E, Turner Syndrome, and acrodysostosisA K Poznanski, E A Werder, A Giedion, et al.
American Journal of Medical Genetics|October 1, 1993
Angel-shaped phalango-epiphyseal dysplasia (ASPED): identification of a new genetic bone markerA Giedion, A Prader, C Fliegel, et al.
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.
Pageof 4