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U Orth

Showing results (1-10 of 40) with videos related to

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Respiration; International Review of Thoracic Diseases|January 1, 1975
Comparative measurements of airway resistanceH Matthys, U Orth
Praxis Der Pneumologie|June 1, 1975
[An electronic digital spirometer (author's transl)]U Orth, H Matthys
Molecular Pathology : MP|June 5, 2003
Three novel PAX6 mutations in patients with aniridiaW Zumkeller, U Orth, A Gal
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1990
[X-chromosomal hereditary night blindness: detection of carriers by segregation analysis with linked DNA markers]U Orth, A Schinzel, M Mächler, et al.
Brain and Language|May 1, 1990
A kinematic analysis of anticipatory coarticulation in the speech of anterior aphasic subjects using electromagnetic articulographyW Katz, J Machetanz, U Orth, et al.
Human Mutation|January 1, 1996
A novel splice-site mutation in the CD40L gene in a patient with X-linked hyper-IgM syndromeD Dezsö, U Orth, H Heilbronner, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 5, 1997
Missense mutation (R15W) of the connexin32 gene in a family with X chromosomal Charcot-Marie-Tooth neuropathy with only female family members affectedE M Wicklein, U Orth, A Gal, et al.
Praxis Und Klinik Der Pneumologie|October 1, 1983
[Bronchofiberscopic catheter and flexible needle suction biopsies in extraluminal and peripheral lung lesion]J A Nakhosteen, L Lindemann, U Orth, et al.
Nature Genetics|August 1, 1994
Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindnessA Gal, U Orth, W Baehr, et al.
Human Genetics|October 1, 1987
A Y/5 translocation in a 45,X male with cri du chat syndromeB Weber, W Schempp, U Orth, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Respiration; International Review of Thoracic Diseases|January 1, 1975
Comparative measurements of airway resistanceH Matthys, U Orth
Praxis Der Pneumologie|June 1, 1975
[An electronic digital spirometer (author's transl)]U Orth, H Matthys
Molecular Pathology : MP|June 5, 2003
Three novel PAX6 mutations in patients with aniridiaW Zumkeller, U Orth, A Gal
Klinische Monatsblatter Fur Augenheilkunde|May 1, 1990
[X-chromosomal hereditary night blindness: detection of carriers by segregation analysis with linked DNA markers]U Orth, A Schinzel, M Mächler, et al.
Brain and Language|May 1, 1990
A kinematic analysis of anticipatory coarticulation in the speech of anterior aphasic subjects using electromagnetic articulographyW Katz, J Machetanz, U Orth, et al.
Human Mutation|January 1, 1996
A novel splice-site mutation in the CD40L gene in a patient with X-linked hyper-IgM syndromeD Dezsö, U Orth, H Heilbronner, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 5, 1997
Missense mutation (R15W) of the connexin32 gene in a family with X chromosomal Charcot-Marie-Tooth neuropathy with only female family members affectedE M Wicklein, U Orth, A Gal, et al.
Praxis Und Klinik Der Pneumologie|October 1, 1983
[Bronchofiberscopic catheter and flexible needle suction biopsies in extraluminal and peripheral lung lesion]J A Nakhosteen, L Lindemann, U Orth, et al.
Nature Genetics|August 1, 1994
Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindnessA Gal, U Orth, W Baehr, et al.
Human Genetics|October 1, 1987
A Y/5 translocation in a 45,X male with cri du chat syndromeB Weber, W Schempp, U Orth, et al.
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