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R M Goodman

Showing results (101-110 of 179) with videos related to

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European Journal of Pediatrics|November 1, 1981
Collagen synthesis by fibroblasts in a patient with the Cockayne syndromeG Keren, D Duksin, B E Cohen, et al.
Clinical Genetics|July 1, 1975
Evidence for an autosomal recessive form of cleidocranial dysostosisR M Goodman, R Tadmor, A Zaritsky, et al.
Clinical Genetics|August 1, 1990
Megalocornea, macrocephaly, mental and motor retardation (MMMM)M Frydman, M Berkenstadt, A Raas-Rothschild, et al.
Harefuah|December 15, 1972
[Biomedical and chromosomal changes in xeroderma pigmentosum: a model of malignant transformation]N Bloch-Shtacher, R M Goodman, T Leu, et al.
Science (New York, N.Y.)|April 3, 1987
Gene transfer in crop improvementR M Goodman, H Hauptli, A Crossway, et al.
Clinical Genetics|November 1, 1987
A new autosomal dominant craniofacial deafness syndromeS Kassutto, Z Kassutto, T Ben-Ami, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1985
Nucleotide sequence of bean golden mosaic virus and a model for gene regulation in geminivirusesA J Howarth, J Caton, M Bossert, et al.
Journal of Medical Genetics|April 1, 1976
Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndromeR M Goodman, M B Katznelson, M Hertz, et al.
American Journal of Medical Genetics|December 15, 1991
New form of postaxial acrofacial dysostosis?R Arens, B Reichman, M B Katznelson, et al.
Clinical Genetics|January 1, 1973
The Wrinkly Skin Syndrome: a new heritable disorder of connective tissueE Gazit, R M Goodman, M B Katznelson, et al.
Pageof 18

Showing results (101-110 of 179) with videos related to

Sort By:
Pageof 18
European Journal of Pediatrics|November 1, 1981
Collagen synthesis by fibroblasts in a patient with the Cockayne syndromeG Keren, D Duksin, B E Cohen, et al.
Clinical Genetics|July 1, 1975
Evidence for an autosomal recessive form of cleidocranial dysostosisR M Goodman, R Tadmor, A Zaritsky, et al.
Clinical Genetics|August 1, 1990
Megalocornea, macrocephaly, mental and motor retardation (MMMM)M Frydman, M Berkenstadt, A Raas-Rothschild, et al.
Harefuah|December 15, 1972
[Biomedical and chromosomal changes in xeroderma pigmentosum: a model of malignant transformation]N Bloch-Shtacher, R M Goodman, T Leu, et al.
Science (New York, N.Y.)|April 3, 1987
Gene transfer in crop improvementR M Goodman, H Hauptli, A Crossway, et al.
Clinical Genetics|November 1, 1987
A new autosomal dominant craniofacial deafness syndromeS Kassutto, Z Kassutto, T Ben-Ami, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1985
Nucleotide sequence of bean golden mosaic virus and a model for gene regulation in geminivirusesA J Howarth, J Caton, M Bossert, et al.
Journal of Medical Genetics|April 1, 1976
Camptodactyly, with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases: Tel Hashomer camptodactyly syndromeR M Goodman, M B Katznelson, M Hertz, et al.
American Journal of Medical Genetics|December 15, 1991
New form of postaxial acrofacial dysostosis?R Arens, B Reichman, M B Katznelson, et al.
Clinical Genetics|January 1, 1973
The Wrinkly Skin Syndrome: a new heritable disorder of connective tissueE Gazit, R M Goodman, M B Katznelson, et al.
Pageof 18