A F Lewanda|E W Jabs - JoVE Visualize

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1991

Analysis of DNA restriction fragments greater than 5.7 Mb in size from the centromeric region of human chromosomesP H Arn, X Li, C Smith, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1983

Ocular histopathology and ultrastructure of Sanfilippo's syndrome, type III-BM A Lavery, W R Green, E W Jabs, et al.

Genomics|August 29, 1998

Human SLUG gene organization, expression, and chromosome map location on 8qM E Cohen, M Yin, W A Paznekas, et al.

American Journal of Medical Genetics|December 14, 1999

Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of "complete ring" syndromeS Sigurdardottir, B K Goodman, J Rutberg, et al.

Human Genetics|May 1, 1994

Chromosomal localization of genes required for the terminal steps of oxidative metabolism: alpha and gamma subunits of ATP synthase and the phosphate carrierE W Jabs, P J Thomas, M Bernstein, et al.

Human Genetics|September 12, 2000

Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC geneJ Boultwood, A J Strickson, E W Jabs, et al.

American Journal of Human Genetics|December 18, 1997

Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locusT D Howard, A E Guttmacher, W McKinnon, et al.

Human Heredity|March 1, 1997

No evidence of linkage for cleft lip with or without cleft palate to a marker near the transforming growth factor alpha locus in two populationsD F Wyszynski, N Maestri, A F Lewanda, et al.

American Journal of Human Genetics|December 1, 1994

Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patientA F Lewanda, E D Green, J Weissenbach, et al.

Genomics|September 1, 1991

Mapping the Treacher Collins syndrome locus to 5q31.3----q33.3E W Jabs, X Li, C A Coss, et al.

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Showing results (31-40 of 109) with videos related to

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Pageof 11

Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1991

Analysis of DNA restriction fragments greater than 5.7 Mb in size from the centromeric region of human chromosomesP H Arn, X Li, C Smith, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1983

Ocular histopathology and ultrastructure of Sanfilippo's syndrome, type III-BM A Lavery, W R Green, E W Jabs, et al.

Genomics|August 29, 1998

Human SLUG gene organization, expression, and chromosome map location on 8qM E Cohen, M Yin, W A Paznekas, et al.

American Journal of Medical Genetics|December 14, 1999

Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of "complete ring" syndromeS Sigurdardottir, B K Goodman, J Rutberg, et al.

Human Genetics|May 1, 1994

Chromosomal localization of genes required for the terminal steps of oxidative metabolism: alpha and gamma subunits of ATP synthase and the phosphate carrierE W Jabs, P J Thomas, M Bernstein, et al.

Human Genetics|September 12, 2000

Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC geneJ Boultwood, A J Strickson, E W Jabs, et al.

American Journal of Human Genetics|December 18, 1997

Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locusT D Howard, A E Guttmacher, W McKinnon, et al.

Human Heredity|March 1, 1997

No evidence of linkage for cleft lip with or without cleft palate to a marker near the transforming growth factor alpha locus in two populationsD F Wyszynski, N Maestri, A F Lewanda, et al.

American Journal of Human Genetics|December 1, 1994

Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patientA F Lewanda, E D Green, J Weissenbach, et al.

Genomics|September 1, 1991

Mapping the Treacher Collins syndrome locus to 5q31.3----q33.3E W Jabs, X Li, C A Coss, et al.

Pageof 11