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U Orth

Showing results (21-30 of 40) with videos related to

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Herz|February 4, 2012
[Hereditary cardiac amyloidosis with transthyretin mutations. A cause of sudden death ]C Edler, W Saeger, U Orth, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|September 28, 2007
[Mutations of the frizzled-4 gene. Their impact on medical care of patients with autosomal dominant exudative vitreoretinopathy]M Müller, C Kusserow, U Orth, et al.
American Journal of Medical Genetics|May 1, 1994
Gene for Simpson-Golabi-Behmel syndrome is linked to HPRT in Xq26 in two European familiesU Orth, F Gurrieri, A Behmel, et al.
Human Genetics|July 1, 1986
X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22M Mächler, D Frey, A Gal, et al.
Clinical Genetics|March 1, 1993
Multipoint linkage analysis in X-linked juvenile retinoschisisA A Bergen, M J van Schooneveld, U Orth, et al.
Prenatal Diagnosis|December 18, 2001
Hydrops fetalis in three male fetuses of a female with incontinentia pigmentiA Dufke, B Vollmer, H Kendziorra, et al.
Neuroscience|April 20, 2005
Mild Pelizaeus-Merzbacher disease caused by a point mutation affecting correct splicing of PLP1 mRNAC A Hübner, A Senning, U Orth, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1990
Posthumous diagnosis of X-linked retinoschisis using DNA analysisM J van Schooneveld, E M Bleeker-Wagemakers, U Orth, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|March 9, 2006
[Inflammatory stage of incontinentia pigmenti (Bloch-Sulzberger syndrome)]A-K Kortüm, A S Büchau, B Assmann, et al.
Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1991
[Autosomal dominant hereditary retinopathia pigmentosa with genetic heterogeneity]U Orth, C Samanns, H Gusseck, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Herz|February 4, 2012
[Hereditary cardiac amyloidosis with transthyretin mutations. A cause of sudden death ]C Edler, W Saeger, U Orth, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|September 28, 2007
[Mutations of the frizzled-4 gene. Their impact on medical care of patients with autosomal dominant exudative vitreoretinopathy]M Müller, C Kusserow, U Orth, et al.
American Journal of Medical Genetics|May 1, 1994
Gene for Simpson-Golabi-Behmel syndrome is linked to HPRT in Xq26 in two European familiesU Orth, F Gurrieri, A Behmel, et al.
Human Genetics|July 1, 1986
X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22M Mächler, D Frey, A Gal, et al.
Clinical Genetics|March 1, 1993
Multipoint linkage analysis in X-linked juvenile retinoschisisA A Bergen, M J van Schooneveld, U Orth, et al.
Prenatal Diagnosis|December 18, 2001
Hydrops fetalis in three male fetuses of a female with incontinentia pigmentiA Dufke, B Vollmer, H Kendziorra, et al.
Neuroscience|April 20, 2005
Mild Pelizaeus-Merzbacher disease caused by a point mutation affecting correct splicing of PLP1 mRNAC A Hübner, A Senning, U Orth, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1990
Posthumous diagnosis of X-linked retinoschisis using DNA analysisM J van Schooneveld, E M Bleeker-Wagemakers, U Orth, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|March 9, 2006
[Inflammatory stage of incontinentia pigmenti (Bloch-Sulzberger syndrome)]A-K Kortüm, A S Büchau, B Assmann, et al.
Fortschritte Der Ophthalmologie : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|January 1, 1991
[Autosomal dominant hereditary retinopathia pigmentosa with genetic heterogeneity]U Orth, C Samanns, H Gusseck, et al.
Pageof 4