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M Opitz

Showing results (441-450 of 520) with videos related to

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American Journal of Medical Genetics|September 1, 1985
Clinicopathological conference: an adolescent girl with severe mental impairment and mucopolysacchariduriaM D Haust, B A Gordon, R Hong, et al.
American Journal of Medical Genetics|July 16, 1999
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?A Bohring, M Silengo, M Lerone, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansionsKlaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
American Journal of Medical Genetics|January 1, 1991
A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six casesM K Bofinger, J M Opitz, S W Soukup, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|August 12, 2004
Comparison of unreamed nailing and external fixation of tibial diastases--mechanical conditions during healing and biological outcomeP Klein, M Opitz, H Schell, et al.
American Journal of Medical Genetics|February 6, 1999
Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: the M syndromeA Rauch, K A Feindt, C O Leonard, et al.
American Journal of Medical Genetics|January 1, 1983
A fifty-year-old man with skin pigmentation, arthritis, chronic renal failure and methemoglobinemiaK Abreo, F Abreo, S W Zimmerman, et al.
American Journal of Medical Genetics. Part A|April 2, 2004
Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndromeFiorella Gurrieri, Gioacchino Scarano, Livia Garavelli, et al.
American Journal of Medical Genetics|July 13, 2002
HOXD13 polyalanine tract expansion in classical synpolydactyly type VordingborgKlaus Wilbrandt Kjaer, Jess Hedeboe, Merete Bugge, et al.
American Journal of Medical Genetics|September 20, 2002
FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]Sabine Dessay, Marie Pierre Moizard, Jean Louis Gilardi, et al.
Pageof 52

Showing results (441-450 of 520) with videos related to

Sort By:
Pageof 52
American Journal of Medical Genetics|September 1, 1985
Clinicopathological conference: an adolescent girl with severe mental impairment and mucopolysacchariduriaM D Haust, B A Gordon, R Hong, et al.
American Journal of Medical Genetics|July 16, 1999
Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?A Bohring, M Silengo, M Lerone, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansionsKlaus W Kjaer, Lars Hansen, Hans Eiberg, et al.
American Journal of Medical Genetics|January 1, 1991
A familial MCA/MR syndrome due to translocation t(10;16) (q26;p13.1): report of six casesM K Bofinger, J M Opitz, S W Soukup, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|August 12, 2004
Comparison of unreamed nailing and external fixation of tibial diastases--mechanical conditions during healing and biological outcomeP Klein, M Opitz, H Schell, et al.
American Journal of Medical Genetics|February 6, 1999
Previously apparently undescribed autosomal recessive MCA/MR syndrome with light fixation, retinal cone dystrophy, and seizures: the M syndromeA Rauch, K A Feindt, C O Leonard, et al.
American Journal of Medical Genetics|January 1, 1983
A fifty-year-old man with skin pigmentation, arthritis, chronic renal failure and methemoglobinemiaK Abreo, F Abreo, S W Zimmerman, et al.
American Journal of Medical Genetics. Part A|April 2, 2004
Mental retardation, Robin sequence, and brachydactyly: further confirmation of a new syndromeFiorella Gurrieri, Gioacchino Scarano, Livia Garavelli, et al.
American Journal of Medical Genetics|July 13, 2002
HOXD13 polyalanine tract expansion in classical synpolydactyly type VordingborgKlaus Wilbrandt Kjaer, Jess Hedeboe, Merete Bugge, et al.
American Journal of Medical Genetics|September 20, 2002
FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]Sabine Dessay, Marie Pierre Moizard, Jean Louis Gilardi, et al.
Pageof 52