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R Kreuz

Showing results (1-10 of 20) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Attitudes of German persons at risk for Huntington's disease toward predictive and prenatal testingF R Kreuz
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Genetic counseling: development of requirements, contents, and quality management in GermanyFriedmar R Kreuz
Clinical Genetics|March 1, 1993
Del(2q)--cause of the wrinkly skin syndrome?F R Kreuz, B H Wittwer
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 20, 2005
[Best's disease with normal EOG. Case report of familial macular dystrophy]K Pollack, F R Kreuz, L E Pillunat
Clinical Dysmorphology|October 26, 1999
Another case of achalasia-microcephaly syndromeF R Kreuz, S Nolte-Buchholtz, F Fackler, et al.
Journal of Neurology|January 13, 2000
Spinocerebellar ataxia type 7: frequency of CAG repeat length in a German familyF R Kreuz, T Grünewald, A Müller, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxiasAndreas Dalski, Jassemien Atici, Friedmar R Kreuz, et al.
Behavior Research Methods, Instruments, & Computers : a Journal of the Psychonomic Society, Inc|June 30, 2000
QUAID: a questionnaire evaluation aid for survey methodologistsA C Graesser, K Wiemer-Hastings, R Kreuz, et al.
Neurology|December 8, 2010
Characteristic MRI and funduscopic findings help diagnose ARSACS outside QuebecM Gerwig, S Krüger, F R Kreuz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 11, 2006
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown causePeter Bauer, Friedmar R Kreuz, Katrin Bürk, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Attitudes of German persons at risk for Huntington's disease toward predictive and prenatal testingF R Kreuz
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Genetic counseling: development of requirements, contents, and quality management in GermanyFriedmar R Kreuz
Clinical Genetics|March 1, 1993
Del(2q)--cause of the wrinkly skin syndrome?F R Kreuz, B H Wittwer
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 20, 2005
[Best's disease with normal EOG. Case report of familial macular dystrophy]K Pollack, F R Kreuz, L E Pillunat
Clinical Dysmorphology|October 26, 1999
Another case of achalasia-microcephaly syndromeF R Kreuz, S Nolte-Buchholtz, F Fackler, et al.
Journal of Neurology|January 13, 2000
Spinocerebellar ataxia type 7: frequency of CAG repeat length in a German familyF R Kreuz, T Grünewald, A Müller, et al.
European Journal of Human Genetics : EJHG|October 8, 2004
Mutation analysis in the fibroblast growth factor 14 gene: frameshift mutation and polymorphisms in patients with inherited ataxiasAndreas Dalski, Jassemien Atici, Friedmar R Kreuz, et al.
Behavior Research Methods, Instruments, & Computers : a Journal of the Psychonomic Society, Inc|June 30, 2000
QUAID: a questionnaire evaluation aid for survey methodologistsA C Graesser, K Wiemer-Hastings, R Kreuz, et al.
Neurology|December 8, 2010
Characteristic MRI and funduscopic findings help diagnose ARSACS outside QuebecM Gerwig, S Krüger, F R Kreuz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 11, 2006
Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown causePeter Bauer, Friedmar R Kreuz, Katrin Bürk, et al.
Pageof 2