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D Steinberger

Showing results (11-20 of 45) with videos related to

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European Journal of Human Genetics : EJHG|October 22, 1998
MEHMO (mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly, obesity), a novel syndrome: assignment of disease locus to xp21.1-p22.13R Steinmüller, D Steinberger, U Müller
Neurogenetics|December 14, 1999
PGL3, a third, not maternally imprinted locus in autosomal dominant paragangliomaS Niemann, D Steinberger, U Müller
Human Mutation|January 1, 1996
Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 geneD Steinberger, J B Mulliken, U Müller
Neurogenetics|March 29, 2000
Clinical and molecular genetics of primary dystoniasU Müller, D Steinberger, A H Németh
Human Genetics|July 1, 1995
Predisposition for cysteine substitutions in the immunoglobulin-like chain of FGFR2 in Crouzon syndromeD Steinberger, J B Mulliken, U Müller
American Journal of Ophthalmology|June 15, 1993
Prevalence of pigment dispersion syndrome in a population undergoing glaucoma screeningR Ritch, D Steinberger, J M Liebmann
American Journal of Medical Genetics|December 2, 1996
FGFR2 mutation in clinically nonclassifiable autosomal dominant craniosynostosis with pronounced phenotypic variationD Steinberger, T Reinhartz, R Unsöld, et al.
Journal of Medical Genetics|May 1, 1997
A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephalyD Steinberger, H Collmann, B Schmalenberger, et al.
Neurology|March 17, 1999
GCH1 mutation in a patient with adult-onset oromandibular dystoniaD Steinberger, H Topka, D Fischer, et al.
Human Genetics|April 1, 1998
The mutations in FGFR2-associated craniosynostoses are clustered in five structural elements of immunoglobulin-like domain III of the receptorD Steinberger, G Vriend, J B Mulliken, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
European Journal of Human Genetics : EJHG|October 22, 1998
MEHMO (mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly, obesity), a novel syndrome: assignment of disease locus to xp21.1-p22.13R Steinmüller, D Steinberger, U Müller
Neurogenetics|December 14, 1999
PGL3, a third, not maternally imprinted locus in autosomal dominant paragangliomaS Niemann, D Steinberger, U Müller
Human Mutation|January 1, 1996
Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 geneD Steinberger, J B Mulliken, U Müller
Neurogenetics|March 29, 2000
Clinical and molecular genetics of primary dystoniasU Müller, D Steinberger, A H Németh
Human Genetics|July 1, 1995
Predisposition for cysteine substitutions in the immunoglobulin-like chain of FGFR2 in Crouzon syndromeD Steinberger, J B Mulliken, U Müller
American Journal of Ophthalmology|June 15, 1993
Prevalence of pigment dispersion syndrome in a population undergoing glaucoma screeningR Ritch, D Steinberger, J M Liebmann
American Journal of Medical Genetics|December 2, 1996
FGFR2 mutation in clinically nonclassifiable autosomal dominant craniosynostosis with pronounced phenotypic variationD Steinberger, T Reinhartz, R Unsöld, et al.
Journal of Medical Genetics|May 1, 1997
A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephalyD Steinberger, H Collmann, B Schmalenberger, et al.
Neurology|March 17, 1999
GCH1 mutation in a patient with adult-onset oromandibular dystoniaD Steinberger, H Topka, D Fischer, et al.
Human Genetics|April 1, 1998
The mutations in FGFR2-associated craniosynostoses are clustered in five structural elements of immunoglobulin-like domain III of the receptorD Steinberger, G Vriend, J B Mulliken, et al.
Pageof 5