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J Spranger

Showing results (131-140 of 247) with videos related to

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Helvetica Paediatrica Acta|December 1, 1985
[Connatal varicella embryo-fetopathy]R König, P Gutjahr, R Kruel, et al.
Neuropediatrics|August 1, 1980
Congenital anomalies in children of epileptic mothers and fathersE Dieterich, A Steveling, A Lukas, et al.
European Journal of Pediatrics|March 1, 1983
Progressive pseudorheumatoid arthritis of childhood (PPAC). A hereditary disorder simulating rheumatoid arthritisJ Spranger, C Albert, F Schilling, et al.
Birth Defects Original Article Series|January 1, 1974
Short rib-polydactyly syndromes and related conditionsJ Spranger, L O Langer, M H Weller, et al.
European Journal of Pediatrics|August 17, 1978
Mucopolysaccharidosis II (Hunter disease) with corneal opacities. Report on two patients at the extremes of a wide clinical spectrumJ Spranger, M Cantz, J Gehler, et al.
Deutsche Medizinische Wochenschrift (1946)|April 21, 2005
[Prevention of type 2 diabetes mellitus. Position paper of the National Action Forum for Diabetes Mellitus]H Hauner, R Landgraf, J Schulze, et al.
Clinical Dysmorphology|January 11, 2001
Ischiospinal dysostosis with rib gaps and nephroblastomatosisJ Spranger, S Self, K B Clarkson, 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.
Pediatric Radiology|January 1, 1994
Kniest dysplasia is caused by dominant collagen II (COL2A1) mutations: parental somatic mosaicism manifesting as Stickler phenotype and mild spondyloepiphyseal dysplasiaJ Spranger, H Menger, S Mundlos, et al.
Klinische Padiatrie|November 1, 1975
[Congenital spondylo-epiphyseal dysplasia: follow-up of a case over 9 years (author's transl)]T Luthardt, H Reinwein, H Schönenberg, et al.
Pageof 25

Showing results (131-140 of 247) with videos related to

Sort By:
Pageof 25
Helvetica Paediatrica Acta|December 1, 1985
[Connatal varicella embryo-fetopathy]R König, P Gutjahr, R Kruel, et al.
Neuropediatrics|August 1, 1980
Congenital anomalies in children of epileptic mothers and fathersE Dieterich, A Steveling, A Lukas, et al.
European Journal of Pediatrics|March 1, 1983
Progressive pseudorheumatoid arthritis of childhood (PPAC). A hereditary disorder simulating rheumatoid arthritisJ Spranger, C Albert, F Schilling, et al.
Birth Defects Original Article Series|January 1, 1974
Short rib-polydactyly syndromes and related conditionsJ Spranger, L O Langer, M H Weller, et al.
European Journal of Pediatrics|August 17, 1978
Mucopolysaccharidosis II (Hunter disease) with corneal opacities. Report on two patients at the extremes of a wide clinical spectrumJ Spranger, M Cantz, J Gehler, et al.
Deutsche Medizinische Wochenschrift (1946)|April 21, 2005
[Prevention of type 2 diabetes mellitus. Position paper of the National Action Forum for Diabetes Mellitus]H Hauner, R Landgraf, J Schulze, et al.
Clinical Dysmorphology|January 11, 2001
Ischiospinal dysostosis with rib gaps and nephroblastomatosisJ Spranger, S Self, K B Clarkson, 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.
Pediatric Radiology|January 1, 1994
Kniest dysplasia is caused by dominant collagen II (COL2A1) mutations: parental somatic mosaicism manifesting as Stickler phenotype and mild spondyloepiphyseal dysplasiaJ Spranger, H Menger, S Mundlos, et al.
Klinische Padiatrie|November 1, 1975
[Congenital spondylo-epiphyseal dysplasia: follow-up of a case over 9 years (author's transl)]T Luthardt, H Reinwein, H Schönenberg, et al.
Pageof 25