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M E Hodes

Showing results (71-80 of 144) with videos related to

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American Journal of Medical Genetics|March 7, 1998
X-linked spastic paraplegia due to a mutation (C506T; Ser169Phe) in exon 4 of the proteolipid protein gene (PLP)M E Hodes, A Hadjisavvas, I J Butler, et al.
American Journal of Medical Genetics|February 1, 1987
Congenital corneal anesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and mental retardation: a new syndrome?M A Ramos-Arroyo, G G Clark, S S Saksena, et al.
American Journal of Diseases of Children (1960)|September 1, 1987
Urorectal septum malformation sequence. Report of six cases and embryological analysisL F Escobar, D D Weaver, D Bixler, et al.
American Journal of Medical Genetics|June 1, 1987
DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNAL Madisen, D I Hoar, C D Holroyd, et al.
Genome Research|August 1, 1996
Direct cDNA selection with DNA microdissected from mouse chromosome 16: isolation of novel clones and construction of a partial transcription map of the C3-C4 regionJ Wei, M E Hodes, Y Wang, et al.
Clinical Genetics|October 7, 2005
Genetic diagnosis of PLP gene duplications/deletions in patients with Pelizaeus-Merzbacher diseaseQ Gao, V C Thurston, G H Vance, et al.
American Journal of Medical Genetics|January 1, 1981
Cartilage-hair hypoplasia, defective T-cell function, and Diamond-Blackfan anemia in an Amish childR E Harris, R L Baehner, S Gleiser, et al.
Neurology|February 1, 1995
A novel mutation in exon 3 of the proteolipid protein gene in Pelizaeus-Merzbacher diseaseV M Pratt, S Naidu, S R Dlouhy, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variantJ A Trofatter, S R Dlouhy, W DeMyer, et al.
American Journal of Medical Genetics|December 1, 1982
Brief clinical report: a child with radius aplasia, cleft of lip and palate, microcephaly, and unusual chromosome findingsM G Butler, L J Russell, C G Palmer, et al.
Pageof 15

Showing results (71-80 of 144) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics|March 7, 1998
X-linked spastic paraplegia due to a mutation (C506T; Ser169Phe) in exon 4 of the proteolipid protein gene (PLP)M E Hodes, A Hadjisavvas, I J Butler, et al.
American Journal of Medical Genetics|February 1, 1987
Congenital corneal anesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and mental retardation: a new syndrome?M A Ramos-Arroyo, G G Clark, S S Saksena, et al.
American Journal of Diseases of Children (1960)|September 1, 1987
Urorectal septum malformation sequence. Report of six cases and embryological analysisL F Escobar, D D Weaver, D Bixler, et al.
American Journal of Medical Genetics|June 1, 1987
DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNAL Madisen, D I Hoar, C D Holroyd, et al.
Genome Research|August 1, 1996
Direct cDNA selection with DNA microdissected from mouse chromosome 16: isolation of novel clones and construction of a partial transcription map of the C3-C4 regionJ Wei, M E Hodes, Y Wang, et al.
Clinical Genetics|October 7, 2005
Genetic diagnosis of PLP gene duplications/deletions in patients with Pelizaeus-Merzbacher diseaseQ Gao, V C Thurston, G H Vance, et al.
American Journal of Medical Genetics|January 1, 1981
Cartilage-hair hypoplasia, defective T-cell function, and Diamond-Blackfan anemia in an Amish childR E Harris, R L Baehner, S Gleiser, et al.
Neurology|February 1, 1995
A novel mutation in exon 3 of the proteolipid protein gene in Pelizaeus-Merzbacher diseaseV M Pratt, S Naidu, S R Dlouhy, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variantJ A Trofatter, S R Dlouhy, W DeMyer, et al.
American Journal of Medical Genetics|December 1, 1982
Brief clinical report: a child with radius aplasia, cleft of lip and palate, microcephaly, and unusual chromosome findingsM G Butler, L J Russell, C G Palmer, et al.
Pageof 15