W B Dobyns|E F Gilbert|J M Opitz - JoVE Visualize

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American Journal of Medical Genetics|January 1, 1981

Idiopathic hydrops fetalis report of 4 patients including 2 affected sibsS M Schwartz, C Viseskul, R Laxova, et al.

Teratology|February 1, 1986

Pulmonary stenosis with ventricular septal defect, common aorticopulmonary trunk, and dextroposition of the aorta: morphologic and qualitative physiologic effects in caffeine-treated chick embryosH J Bruyere, T Nishikawa, H Uno, et al.

Nature Genetics|January 1, 1997

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channelO Zhuchenko, J Bailey, P Bonnen, et al.

American Journal of Medical Genetics|February 1, 1989

Diagnostic criteria for Walker-Warburg syndromeW B Dobyns, R A Pagon, D Armstrong, et al.

American Journal of Human Genetics|October 11, 1992

Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhereH Northrup, D J Kwiatkowski, E S Roach, et al.

American Journal of Medical Genetics|April 14, 1997

Another "new" form, the palagonia type of acrofacial dysostosis in a Sicilian familyG Sorge, L Pavone, A Polizzi, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972

Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.

American Journal of Medical Genetics|November 1, 1994

Microcephaly, lymphedema, and chorioretinal dysplasia: report of two additional casesB Angle, S Holgado, B K Burton, et al.

Neurology|August 3, 1999

Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephalyW B Dobyns, C L Truwit, M E Ross, et al.

American Journal of Medical Genetics|July 1, 1986

Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndromeR F Stratton, W B Dobyns, F Greenberg, et al.

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Showing results (281-290 of 392) with videos related to

Sort By:

Pageof 40

American Journal of Medical Genetics|January 1, 1981

Idiopathic hydrops fetalis report of 4 patients including 2 affected sibsS M Schwartz, C Viseskul, R Laxova, et al.

Teratology|February 1, 1986

Pulmonary stenosis with ventricular septal defect, common aorticopulmonary trunk, and dextroposition of the aorta: morphologic and qualitative physiologic effects in caffeine-treated chick embryosH J Bruyere, T Nishikawa, H Uno, et al.

Nature Genetics|January 1, 1997

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channelO Zhuchenko, J Bailey, P Bonnen, et al.

American Journal of Medical Genetics|February 1, 1989

Diagnostic criteria for Walker-Warburg syndromeW B Dobyns, R A Pagon, D Armstrong, et al.

American Journal of Human Genetics|October 11, 1992

Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhereH Northrup, D J Kwiatkowski, E S Roach, et al.

American Journal of Medical Genetics|April 14, 1997

Another "new" form, the palagonia type of acrofacial dysostosis in a Sicilian familyG Sorge, L Pavone, A Polizzi, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972

Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.

American Journal of Medical Genetics|November 1, 1994

Microcephaly, lymphedema, and chorioretinal dysplasia: report of two additional casesB Angle, S Holgado, B K Burton, et al.

Neurology|August 3, 1999

Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephalyW B Dobyns, C L Truwit, M E Ross, et al.

American Journal of Medical Genetics|July 1, 1986

Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndromeR F Stratton, W B Dobyns, F Greenberg, et al.

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