D T Bishop|S L Sherman - JoVE Visualize

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Genomics|February 1, 1991

Fanconi anemia: evidence for linkage heterogeneity on chromosome 20qW R Mann, V S Venkatraj, R G Allen, et al.

American Journal of Human Genetics|December 5, 1998

Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severityI D Waldman, D C Rowe, A Abramowitz, et al.

The British Journal of Dermatology|July 27, 2011

The determinants of periorbital skin ageing in participants of a melanoma case-control study in the U.KM Suppa, F Elliott, J S Mikeljevic, et al.

Human Genetics|January 1, 1985

Further segregation analysis of the fragile X syndrome with special reference to transmitting malesS L Sherman, P A Jacobs, N E Morton, et al.

American Journal of Medical Genetics|April 1, 1992

Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X siteG J Riggins, S L Sherman, B A Oostra, et al.

American Journal of Medical Genetics|February 1, 1991

Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell culturesE C Jenkins, M S Krawczun, S L Stark-Houck, et al.

Human Molecular Genetics|July 21, 1998

Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humansA R Savage, M B Petersen, D Pettay, et al.

Human Reproduction (Oxford, England)|May 18, 2011

Intra-individual stability over time of standardized anti-Mullerian hormone in FMR1 premutation carriersM A Spath, T B Feuth, E G Allen, et al.

Human Reproduction (Oxford, England)|November 6, 2015

Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiencyR A M Buijsen, J A Visser, P Kramer, et al.

Human Molecular Genetics|November 13, 1998

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1C Gunter, W Paradee, D C Crawford, et al.

Pageof 23

Showing results (191-200 of 222) with videos related to

Sort By:

Pageof 23

Genomics|February 1, 1991

Fanconi anemia: evidence for linkage heterogeneity on chromosome 20qW R Mann, V S Venkatraj, R G Allen, et al.

American Journal of Human Genetics|December 5, 1998

Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severityI D Waldman, D C Rowe, A Abramowitz, et al.

The British Journal of Dermatology|July 27, 2011

The determinants of periorbital skin ageing in participants of a melanoma case-control study in the U.KM Suppa, F Elliott, J S Mikeljevic, et al.

Human Genetics|January 1, 1985

Further segregation analysis of the fragile X syndrome with special reference to transmitting malesS L Sherman, P A Jacobs, N E Morton, et al.

American Journal of Medical Genetics|April 1, 1992

Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X siteG J Riggins, S L Sherman, B A Oostra, et al.

American Journal of Medical Genetics|February 1, 1991

Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell culturesE C Jenkins, M S Krawczun, S L Stark-Houck, et al.

Human Molecular Genetics|July 21, 1998

Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humansA R Savage, M B Petersen, D Pettay, et al.

Human Reproduction (Oxford, England)|May 18, 2011

Intra-individual stability over time of standardized anti-Mullerian hormone in FMR1 premutation carriersM A Spath, T B Feuth, E G Allen, et al.

Human Reproduction (Oxford, England)|November 6, 2015

Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiencyR A M Buijsen, J A Visser, P Kramer, et al.

Human Molecular Genetics|November 13, 1998

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1C Gunter, W Paradee, D C Crawford, et al.

Pageof 23