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P. K. Jensen

American journal of medical genetics, Circulation, American Heart Journal, Circulation: Cardiovascular Genetics, Ophthalmic Genetics, Cancer Genetics and Cytogenetics, American Journal of Human Genetics, Genetic Testing Show more
9
Role
Title
Level Year L/R
🐬 Recurrence of Congenital Heart Defects in Families
N. Øyen, G. Poulsen, H. Boyd, J. Wohlfahrt, P. K. Jensen, M. Melbye 		8 2009
8
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🐬 National time trends in congenital heart defects, Denmark, 1977-2005.
N. Oyen, G. Poulsen, H. Boyd, J. Wohlfahrt, P. K. Jensen, M. Melbye 		7 2009
7
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🐬 Recurrence of Discordant Congenital Heart Defects in Families
N. Øyen, G. Poulsen, J. Wohlfahrt, H. Boyd, P. K. Jensen, M. Melbye 		6 2010
6
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🐜 Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a gene
11 auth. L. Tranebjærg, P. K. Jensen, M. Van Ghelue, C. Vnencak-Jones, Staale Sund, K. Elgjo, ... Johannes Jakobsen, S. Lindal, M. Warburg, A. Fuglsang-Frederiksen, K. Skullerud 		5 2001
5
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🐬 Low frequency of large genomic rearrangements of BRCA1 and BRCA2 in western Denmark.
M. Thomassen, A. Gerdes, D. Cruger, P. K. Jensen, T. Kruse 		5 2006
5
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🐬 Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation.
R. Plenge, L. Tranebjaerg, P. K. Jensen, C. Schwartz, H. Willard 		5 1999
5
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🦁 The syndrome of opticoacoustic nerve atrophy with dementia.
P. K. Jensen, E. Reske‐Nielsen, O. Hein-Sørensen, M. Warburg 		4 1987
4
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🦁 Nerve deafness: optic nerve atrophy, and dementia: a new X-linked recessive syndrome?
P. K. Jensen 		3 1981
3
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🐬 A missense mutation in exon 13 in BRCA2, c.7235G>A, results in skipping of exon 13.
M. Thomassen, T. Kruse, P. K. Jensen, A. Gerdes 		3 2006
3
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