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P Steinbach

Showing results (1-10 of 369) with videos related to

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Cell and Tissue Research|June 20, 1977
Granular cells in the connective tissue of Helix pomatia L. (gastropoda, pulmonata). Histochemistry, ultrastructure, and results of polyacrylamide electrophoretic investigationsP Steinbach
Human Genetics|March 1, 1986
Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosomeP Steinbach
Human Genetics|August 1, 1986
Excess of mental retardation and/or congenital malformation in reciprocal translocations in manP Steinbach
American Journal of Medical Genetics|October 1, 1985
Fragile X and Martin-Bell syndrome: new source of informationG Barbi, P Steinbach
Human Genetics|August 1, 1991
Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardationD Wöhrle, P Steinbach
Human Genetics|January 1, 1982
Increase in the incidence of the fragile site Xq27 in prometaphasesG Barbi, P Steinbach
Human Genetics|January 1, 1983
Demonstration of gene dosage effects for AK3 and GALT in fibroblasts from a fetus with 9p trisomyP Steinbach, R Benz
Human Genetics|January 1, 1983
Ineffectivity of accessory bisatellited marker chromosomes in inducing meiotic nondisjunctionP Steinbach, M Djalali
Clinical Genetics|July 1, 1987
Tetrasomy for the short arm of chromosome 12 with accessory isochromosome (+i(12p)) and a marked LDH-B gene dosage effectP Steinbach, H Rehder
Caring : National Association for Home Care Magazine|February 7, 1996
Restoring the Medicaid hospice benefit in IllinoisM Kulczycki, P Steinbach
Pageof 37

Showing results (1-10 of 369) with videos related to

Sort By:
Pageof 37
Cell and Tissue Research|June 20, 1977
Granular cells in the connective tissue of Helix pomatia L. (gastropoda, pulmonata). Histochemistry, ultrastructure, and results of polyacrylamide electrophoretic investigationsP Steinbach
Human Genetics|March 1, 1986
Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosomeP Steinbach
Human Genetics|August 1, 1986
Excess of mental retardation and/or congenital malformation in reciprocal translocations in manP Steinbach
American Journal of Medical Genetics|October 1, 1985
Fragile X and Martin-Bell syndrome: new source of informationG Barbi, P Steinbach
Human Genetics|August 1, 1991
Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardationD Wöhrle, P Steinbach
Human Genetics|January 1, 1982
Increase in the incidence of the fragile site Xq27 in prometaphasesG Barbi, P Steinbach
Human Genetics|January 1, 1983
Demonstration of gene dosage effects for AK3 and GALT in fibroblasts from a fetus with 9p trisomyP Steinbach, R Benz
Human Genetics|January 1, 1983
Ineffectivity of accessory bisatellited marker chromosomes in inducing meiotic nondisjunctionP Steinbach, M Djalali
Clinical Genetics|July 1, 1987
Tetrasomy for the short arm of chromosome 12 with accessory isochromosome (+i(12p)) and a marked LDH-B gene dosage effectP Steinbach, H Rehder
Caring : National Association for Home Care Magazine|February 7, 1996
Restoring the Medicaid hospice benefit in IllinoisM Kulczycki, P Steinbach
Pageof 37