E L Bingham - JoVE Visualize

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Human Heredity|November 1, 1996

X-linked juvenile retinoschisis: localization between (DXS1195, DXS418) and AFM291wf5 on a single YACH Pawar, E L Bingham, K Hiriyanna, et al.

The American Journal of Pathology|May 1, 1988

Rearrangement of immunoglobulin and T-cell receptor genes in Hodgkin's diseaseM S Roth, B Schnitzer, E L Bingham, et al.

Molecular Vision|July 31, 1999

Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment geneR Ayyagari, L E Kakuk, C L Coats, et al.

Human Heredity|July 1, 1995

Refined genetic mapping of juvenile X-linked retinoschisisH Pawar, E L Bingham, K L Lunetta, et al.

American Journal of Human Genetics|October 1, 1990

Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probesP A Sieving, E L Bingham, M S Roth, et al.

Human Genetics|September 12, 2000

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacyR Ayyagari, L E Kakuk, E L Bingham, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|August 2, 2000

Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 geneL C Eksandh, V Ponjavic, R Ayyagari, et al.

Ophthalmic Genetics|July 23, 1999

A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutationR Mendoza-Londono, K T Hiriyanna, E L Bingham, et al.

Human Heredity|July 1, 1996

Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American familyY C Hou, J E Richards, E L Bingham, et al.

Genomics|March 2, 1999

Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22S M Walpole, K T Hiriyana, A Nicolaou, et al.

Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:

Pageof 3

Human Heredity|November 1, 1996

X-linked juvenile retinoschisis: localization between (DXS1195, DXS418) and AFM291wf5 on a single YACH Pawar, E L Bingham, K Hiriyanna, et al.

The American Journal of Pathology|May 1, 1988

Rearrangement of immunoglobulin and T-cell receptor genes in Hodgkin's diseaseM S Roth, B Schnitzer, E L Bingham, et al.

Molecular Vision|July 31, 1999

Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment geneR Ayyagari, L E Kakuk, C L Coats, et al.

Human Heredity|July 1, 1995

Refined genetic mapping of juvenile X-linked retinoschisisH Pawar, E L Bingham, K L Lunetta, et al.

American Journal of Human Genetics|October 1, 1990

Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probesP A Sieving, E L Bingham, M S Roth, et al.

Human Genetics|September 12, 2000

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacyR Ayyagari, L E Kakuk, E L Bingham, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|August 2, 2000

Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 geneL C Eksandh, V Ponjavic, R Ayyagari, et al.

Ophthalmic Genetics|July 23, 1999

A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutationR Mendoza-Londono, K T Hiriyanna, E L Bingham, et al.

Human Heredity|July 1, 1996

Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American familyY C Hou, J E Richards, E L Bingham, et al.

Genomics|March 2, 1999

Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22S M Walpole, K T Hiriyana, A Nicolaou, et al.

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