H H Ropers - JoVE Visualize

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Genomics|October 1, 1989

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19H G Brunner, H Smeets, H M Lambermon, et al.

American Journal of Medical Genetics|April 10, 1995

Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier reportB C Hamel, J M Draaisma, A J Pinckers, et al.

Human Genetics|August 1, 1993

Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1E C Mariman, A A Gabreëls-Festen, S E van Beersum, et al.

American Journal of Human Genetics|March 1, 1984

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybridsP Wieacker, K E Davies, H J Cooke, et al.

Biochemical and Biophysical Research Communications|May 16, 1998

Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expressionA M Riesewijk, Y Q Xu, M T Schepens, et al.

Human Genetics|December 1, 1994

Location of the gene causing hyperimmunoglobulinemia D and periodic fever syndrome differs from that for familial Mediterranean fever. International Hyper-IgD Study GroupJ P Drenth, E C Mariman, S D Van der Velde-Visser, et al.

Clinical Genetics|December 1, 1987

Deletion of the DXS165 locus in patients with classical choroideremiaF P Cremers, F Brunsmann, T J van de Pol, et al.

Human Molecular Genetics|July 13, 1999

RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosaR Kirschner, T Rosenberg, R Schultz-Heienbrok, et al.

Human Molecular Genetics|August 25, 2000

The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptorsR Roepman, N Bernoud-Hubac, D E Schick, et al.

Genomics|January 1, 1989

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromesF P Cremers, D J van de Pol, P J Diergaarde, et al.

Pageof 21

Showing results (111-120 of 204) with videos related to

Sort By:

Pageof 21

Genomics|October 1, 1989

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19H G Brunner, H Smeets, H M Lambermon, et al.

American Journal of Medical Genetics|April 10, 1995

Autosomal recessive Melnick-Needles syndrome or ter Haar syndrome? Report of a patient and reappraisal of an earlier reportB C Hamel, J M Draaisma, A J Pinckers, et al.

Human Genetics|August 1, 1993

Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1E C Mariman, A A Gabreëls-Festen, S E van Beersum, et al.

American Journal of Human Genetics|March 1, 1984

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybridsP Wieacker, K E Davies, H J Cooke, et al.

Biochemical and Biophysical Research Communications|May 16, 1998

Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expressionA M Riesewijk, Y Q Xu, M T Schepens, et al.

Human Genetics|December 1, 1994

Location of the gene causing hyperimmunoglobulinemia D and periodic fever syndrome differs from that for familial Mediterranean fever. International Hyper-IgD Study GroupJ P Drenth, E C Mariman, S D Van der Velde-Visser, et al.

Clinical Genetics|December 1, 1987

Deletion of the DXS165 locus in patients with classical choroideremiaF P Cremers, F Brunsmann, T J van de Pol, et al.

Human Molecular Genetics|July 13, 1999

RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosaR Kirschner, T Rosenberg, R Schultz-Heienbrok, et al.

Human Molecular Genetics|August 25, 2000

The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptorsR Roepman, N Bernoud-Hubac, D E Schick, et al.

Genomics|January 1, 1989

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromesF P Cremers, D J van de Pol, P J Diergaarde, et al.

Pageof 21