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M E Hodes

Showing results (51-60 of 144) with videos related to

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Journal of Clinical Immunology|April 1, 1983
Immunologic studies of three family members with the immunodeficiency with hyper-IgM syndromeZ Brahmi, K H Lazarus, M E Hodes, et al.
Human Genetics|January 1, 1982
The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromesR S Young, T Reed, M E Hodes, et al.
Neurology|April 1, 1987
X-linked recessive inheritance of ataxia and adult-onset dementia: clinical features and preliminary linkage analysisM R Farlow, W DeMyer, S R Dlouhy, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuriaS Naidu, S R Dlouhy, M T Geraghty, et al.
Human Pathology|November 1, 1983
Immunohistochemical demonstration of ribonuclease and amylase in normal and neoplastic parotid glandsD J Morley, J E Hodes, J Calland, et al.
Analytical Biochemistry|July 15, 1979
A positive zymogram method for ribonucleaseR C Karn, M Crisp, E A Yount, et al.
Journal of Medical Genetics|February 1, 1978
Genetic family history questionnaireJ Cole, P M Conneally, M E Hodes, et al.
Birth Defects Original Article Series|January 1, 1978
The utilization of a written family history questionnaire in genetic counselingJ Cole, M P Conneally, M E Hodes, et al.
Genomics|May 15, 1996
Cloning a cDNA for carbonyl reductase (Cbr) from mouse cerebellum: murine genes that express cbr map to chromosomes 16 and 11J Wei, S R Dlouhy, A Hara, et al.
Nucleic Acids Research|November 11, 1991
AhaII polymorphism in human X-linked proteolipid protein gene (PLP)J A Trofatter, V M Pratt, S R Dlouhy, et al.
Pageof 15

Showing results (51-60 of 144) with videos related to

Sort By:
Pageof 15
Journal of Clinical Immunology|April 1, 1983
Immunologic studies of three family members with the immunodeficiency with hyper-IgM syndromeZ Brahmi, K H Lazarus, M E Hodes, et al.
Human Genetics|January 1, 1982
The dermatoglyphic and clinical features of the 9p trisomy and partial 9p monosomy syndromesR S Young, T Reed, M E Hodes, et al.
Neurology|April 1, 1987
X-linked recessive inheritance of ataxia and adult-onset dementia: clinical features and preliminary linkage analysisM R Farlow, W DeMyer, S R Dlouhy, et al.
Journal of Inherited Metabolic Disease|January 14, 1998
A male child with the rumpshaker mutation, X-linked spastic paraplegia/Pelizaeus-Merzbacher disease and lysinuriaS Naidu, S R Dlouhy, M T Geraghty, et al.
Human Pathology|November 1, 1983
Immunohistochemical demonstration of ribonuclease and amylase in normal and neoplastic parotid glandsD J Morley, J E Hodes, J Calland, et al.
Analytical Biochemistry|July 15, 1979
A positive zymogram method for ribonucleaseR C Karn, M Crisp, E A Yount, et al.
Journal of Medical Genetics|February 1, 1978
Genetic family history questionnaireJ Cole, P M Conneally, M E Hodes, et al.
Birth Defects Original Article Series|January 1, 1978
The utilization of a written family history questionnaire in genetic counselingJ Cole, M P Conneally, M E Hodes, et al.
Genomics|May 15, 1996
Cloning a cDNA for carbonyl reductase (Cbr) from mouse cerebellum: murine genes that express cbr map to chromosomes 16 and 11J Wei, S R Dlouhy, A Hara, et al.
Nucleic Acids Research|November 11, 1991
AhaII polymorphism in human X-linked proteolipid protein gene (PLP)J A Trofatter, V M Pratt, S R Dlouhy, et al.
Pageof 15