F Greenberg|D H Ledbetter - JoVE Visualize

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Journal of Medical Genetics|July 25, 1998

Molecular screening for proximal 15q abnormalities in a mentally retarded populationJ Jacobsen, B H King, B L Leventhal, et al.

Genes, Chromosomes & Cancer|March 1, 1994

Detailed analysis of loss of heterozygosity on chromosome band 17p13 in breast carcinoma on the basis of a high-resolution physical map with 29 markersM Isomura, A Tanigami, H Saito, et al.

Oncogene|January 1, 1987

Localization of myeloperoxidase to the long arm of human chromosome 17: relationship to the 15; 17 translocation of acute promyelocytic leukemiaP van Tuinen, K R Johnson, S A Ledbetter, et al.

Human Molecular Genetics|February 1, 1997

Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeC Lo Nigro, C S Chong, A C Smith, et al.

The Journal of Pediatrics|May 1, 1995

Dysmorphic features in patients with complex glycerol kinase deficiencyA Scheuerle, F Greenberg, E R McCabe

American Journal of Medical Genetics|May 1, 1989

Weaver syndrome: the changing phenotype in an adultF Greenberg, W Wasiewski, E R McCabe

American Journal of Medical Genetics|June 5, 1998

Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2)A C Smith, E Dykens, F Greenberg

Proceedings of the National Academy of Sciences of the United States of America|July 1, 1991

Genetic analysis of indefinite division in human cells: evidence for a cell senescence-related gene(s) on human chromosome 4Y Ning, J L Weber, A M Killary, et al.

American Journal of Human Genetics|January 1, 1997

Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardationA C Wong, Y Ning, J Flint, et al.

American Journal of Respiratory Cell and Molecular Biology|July 1, 1992

An unusual expression of a squamous cell marker, small proline-rich protein gene, in tracheobronchial epithelium: differential regulation and gene mappingG An, T H Huang, J Tesfaigzi, et al.

Pageof 33

Showing results (131-140 of 324) with videos related to

Sort By:

Pageof 33

Journal of Medical Genetics|July 25, 1998

Molecular screening for proximal 15q abnormalities in a mentally retarded populationJ Jacobsen, B H King, B L Leventhal, et al.

Genes, Chromosomes & Cancer|March 1, 1994

Detailed analysis of loss of heterozygosity on chromosome band 17p13 in breast carcinoma on the basis of a high-resolution physical map with 29 markersM Isomura, A Tanigami, H Saito, et al.

Oncogene|January 1, 1987

Localization of myeloperoxidase to the long arm of human chromosome 17: relationship to the 15; 17 translocation of acute promyelocytic leukemiaP van Tuinen, K R Johnson, S A Ledbetter, et al.

Human Molecular Genetics|February 1, 1997

Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndromeC Lo Nigro, C S Chong, A C Smith, et al.

The Journal of Pediatrics|May 1, 1995

Dysmorphic features in patients with complex glycerol kinase deficiencyA Scheuerle, F Greenberg, E R McCabe

American Journal of Medical Genetics|May 1, 1989

Weaver syndrome: the changing phenotype in an adultF Greenberg, W Wasiewski, E R McCabe

American Journal of Medical Genetics|June 5, 1998

Behavioral phenotype of Smith-Magenis syndrome (del 17p11.2)A C Smith, E Dykens, F Greenberg

Proceedings of the National Academy of Sciences of the United States of America|July 1, 1991

Genetic analysis of indefinite division in human cells: evidence for a cell senescence-related gene(s) on human chromosome 4Y Ning, J L Weber, A M Killary, et al.

American Journal of Human Genetics|January 1, 1997

Molecular characterization of a 130-kb terminal microdeletion at 22q in a child with mild mental retardationA C Wong, Y Ning, J Flint, et al.

American Journal of Respiratory Cell and Molecular Biology|July 1, 1992

An unusual expression of a squamous cell marker, small proline-rich protein gene, in tracheobronchial epithelium: differential regulation and gene mappingG An, T H Huang, J Tesfaigzi, et al.

Pageof 33