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Nature Genetics
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April 1, 1992
Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A
J R Lupski, C A Wise, A Kuwano, et al.
The Journal of Biological Chemistry
|
December 5, 1998
Human 12(R)-lipoxygenase and the mouse ortholog. Molecular cloning, expression, and gene chromosomal assignment
D Sun, M McDonnell, X S Chen, et al.
American Journal of Medical Genetics
|
September 15, 1993
Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion
R T Zori, J R Lupski, Z Heju, et al.
The Journal of Biological Chemistry
|
October 14, 1994
Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters
U Suter, G J Snipes, R Schoener-Scott, et al.
Human Genetics
|
July 1, 1991
Molecular characterization of a patient with del(1)(q23-q25)
B Franco, L W Lai, D Patterson, et al.
Genomics
|
July 1, 1992
Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p
V Guzzetta, B Franco, B J Trask, et al.
American Journal of Human Genetics
|
December 1, 1991
Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2)
F Greenberg, V Guzzetta, R Montes de Oca-Luna, et al.
Clinical Genetics
|
March 30, 2011
A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia
G A Mendoza-Fandino, J M Gee, S Ben-Dor, et al.
The New England Journal of Medicine
|
July 8, 1993
Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene
B B Roa, C A Garcia, U Suter, et al.
Nature Genetics
|
October 1, 1993
Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1A
B B Roa, C A Garcia, L Pentao, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 85) with videos related to
Sort By:
Page
of 9
Nature Genetics
|
April 1, 1992
Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A
J R Lupski, C A Wise, A Kuwano, et al.
The Journal of Biological Chemistry
|
December 5, 1998
Human 12(R)-lipoxygenase and the mouse ortholog. Molecular cloning, expression, and gene chromosomal assignment
D Sun, M McDonnell, X S Chen, et al.
American Journal of Medical Genetics
|
September 15, 1993
Clinical, cytogenetic, and molecular evidence for an infant with Smith-Magenis syndrome born from a mother having a mosaic 17p11.2p12 deletion
R T Zori, J R Lupski, Z Heju, et al.
The Journal of Biological Chemistry
|
October 14, 1994
Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters
U Suter, G J Snipes, R Schoener-Scott, et al.
Human Genetics
|
July 1, 1991
Molecular characterization of a patient with del(1)(q23-q25)
B Franco, L W Lai, D Patterson, et al.
Genomics
|
July 1, 1992
Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p
V Guzzetta, B Franco, B J Trask, et al.
American Journal of Human Genetics
|
December 1, 1991
Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2)
F Greenberg, V Guzzetta, R Montes de Oca-Luna, et al.
Clinical Genetics
|
March 30, 2011
A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia
G A Mendoza-Fandino, J M Gee, S Ben-Dor, et al.
The New England Journal of Medicine
|
July 8, 1993
Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene
B B Roa, C A Garcia, U Suter, et al.
Nature Genetics
|
October 1, 1993
Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1A
B B Roa, C A Garcia, L Pentao, et al.
Page
of 9