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Results : 26-50/195

Simultaneous effects of the apolipoprotein E polymorphism on apolipoprotein E, apolipoprotein B, and cholesterol metabolism

Authors: Boerwinkle, Eric Utermann, Gerd

Journal: American journal of human genetics

Citation: Boerwinkle, Eric et Utermann, Gerd, Simultaneous effects of the apolipoprotein E polymorphism on apolipoprotein E, apolipoprotein B, and cholesterol metabolism, American journal of human genetics , 42(1), 1988, pp. 104-112

The detection of linkage disequilibrium between closely linked markers: RFLPs at the Al-ClII apolipoprotein genes

Authors: Thompson, E. A. Deeb, S. Walker, D. Motulsky, A. G.

Journal: American journal of human genetics

Citation: A. Thompson, E. et al., The detection of linkage disequilibrium between closely linked markers: RFLPs at the Al-ClII apolipoprotein genes, American journal of human genetics , 42(1), 1988, pp. 113-124

A Genetical model for vitiligo

Authors: Majumder, Partha P. Das, S. K. Li, C. C.

Journal: American journal of human genetics

Citation: P. Majumder, Partha et al., A Genetical model for vitiligo, American journal of human genetics , 43-I(2), 1988, pp. 119-125

A polymorphic DNA marker that represents a conserved expressed sequence in the region of the huntington disease gene

Authors: Hayden, Michael R. Hewitt, Jeffrey Wasmuth, John J. Kastelein, Jan J. Langlois,Sylvie Conneally, Michael Haines, Jonathan Smith, Barbara Hilbert, Chantal Allard, Denis

Journal: American journal of human genetics

Citation: R. Hayden, Michael et al., A polymorphic DNA marker that represents a conserved expressed sequence in the region of the huntington disease gene, American journal of human genetics , 42(1), 1988, pp. 125-131

Myopathy in complex glycerol kinase deficiency patients is due to 3' deletions of the dystrophin gene

Authors: Darras, Basil T. Francke, Uta

Journal: American journal of human genetics

Citation: T. Darras, Basil et Francke, Uta, Myopathy in complex glycerol kinase deficiency patients is due to 3' deletions of the dystrophin gene, American journal of human genetics , 43-I(2), 1988, pp. 126-130

The same extra fokI cleavage site exists in glucose-6-phosphate dehydrogenase variants A(+ ) and A(-)

Authors: Yoshida, Akra Takizawa, Takenori

Journal: American journal of human genetics

Citation: Yoshida, Akra et Takizawa, Takenori, The same extra fokI cleavage site exists in glucose-6-phosphate dehydrogenase variants A(+ ) and A(-), American journal of human genetics , 43-I(2), 1988, pp. 131-133

HLA and the probability of paternity

Authors: Richard Borowsky

Journal: American journal of human genetics

Citation: Richard Borowsky, HLA and the probability of paternity, American journal of human genetics , 42(1), 1988, pp. 132-134

Mitochondrial DNA polymorphism among five asian populations

Authors: Harihara, S. Gojobori, T. Hirai, M. Saitou, N. Park, K. S. Misawa, S. Ellepola, S. B. Ishida, T. Omoto, K.

Journal: American journal of human genetics

Citation: S. Harihara, et al., Mitochondrial DNA polymorphism among five asian populations, American journal of human genetics , 43-I(2), 1988, pp. 134-143

Bayesian Interval Estimation of Genetic Relationships: Application to Paternity Testing

Authors: Goldgar, David E. Thompson, Elizabeth A.

Journal: American journal of human genetics

Citation: E. Goldgar, David et A. Thompson, Elizabeth, Bayesian Interval Estimation of Genetic Relationships: Application to Paternity Testing, American journal of human genetics , 42(1), 1988, pp. 135-142

Identification of more than 500 RFLPs by screening random genomic clones

Authors: Schumm, James W. Knowlton, Robert G. Braman, Jeffrey C. Barker, David F. Botstein, David Akots, Gita Brown, Valerie A. Gravius, Thomas C. Helms, Cynthia Hsiao, Kathy Rediker, Kenneth Thurston, Joan G. Donis-Keller, Helen

Journal: American journal of human genetics

Citation: W. Schumm, James et al., Identification of more than 500 RFLPs by screening random genomic clones, American journal of human genetics , 42(1), 1988, pp. 143-159

Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair

Authors: Stallings, Raymond L. Olson, Eric Strauss, Arnold W. Thompson, Larry H. Bachinski, Linda L. Siciliano, Michael j.

Journal: American journal of human genetics

Citation: L. Stallings, Raymond et al., Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair, American journal of human genetics , 43-I(2), 1988, pp. 144-152

Human pregnancy-specific beta I glycoprotein is encoded by multiple genes localized on two chromosomes

Authors: Chan, Wai-Yee Qiu, Wan-Rong

Journal: American journal of human genetics

Citation: Chan, Wai-yee et Qiu, Wan-rong, Human pregnancy-specific beta I glycoprotein is encoded by multiple genes localized on two chromosomes, American journal of human genetics , 43-I(2), 1988, pp. 152-159

Linkage of a gene regulating dopamine-beta-hydroxylase activity and the ABO blood group locus

Authors: Wilson, A. F. Elston, R. C. Siervogel, R. M. Tran, L. D.

Journal: American journal of human genetics

Citation: F. Wilson, A. et al., Linkage of a gene regulating dopamine-beta-hydroxylase activity and the ABO blood group locus, American journal of human genetics , 42(1), 1988, pp. 160-166

Variability in predicted rates of down syndrome associated with elevated maternal serum alpha-fetoprotein levels in older women

Authors: Hook, Ernest B.

Journal: American journal of human genetics

Citation: B. Hook, Ernest, Variability in predicted rates of down syndrome associated with elevated maternal serum alpha-fetoprotein levels in older women, American journal of human genetics , 43-I(2), 1988, pp. 160-164

Oresomucoid (ORM) typing by isoelectric focusing: evidence for an additional duplicated ORM I locus maplotype and close linkage of two ORM lod

Authors: Yuasa, isao Urnetsu, Kazuo Suenaga, Kazuyuki

Journal: American journal of human genetics

Citation: Yuasa, Isao et al., Oresomucoid (ORM) typing by isoelectric focusing: evidence for an additional duplicated ORM I locus maplotype and close linkage of two ORM lod, American journal of human genetics , 43-I(2), 1988, pp. 165-169

Insulin-Gene Sharing in Sib Pairs with Insulin-Dependent Diabetes Mellitus: No Evidence for Linkage

Authors: Cox, Nancy J. Baker, Lester Spielman, Richard S.

Journal: American journal of human genetics

Citation: J. Cox, Nancy et al., Insulin-Gene Sharing in Sib Pairs with Insulin-Dependent Diabetes Mellitus: No Evidence for Linkage, American journal of human genetics , 42(1), 1988, pp. 167-172

Polymorphism of the a subunit of coagulation factor XIII: evidence for subtypes of the FXIIIA 1 and FXIIIA 2 Alleles

Authors: Suzuki, Koichi Matsui, Kiyoshi Ito, Shigenori Fujita, Kiyoshi Matsumoto, Hideo

Journal: American journal of human genetics

Citation: Suzuki, Koichi et al., Polymorphism of the a subunit of coagulation factor XIII: evidence for subtypes of the FXIIIA 1 and FXIIIA 2 Alleles, American journal of human genetics , 43-I(2), 1988, pp. 170-174

Alternative Bioassays of Kinship between Loci

Authors: Morton, N. E. Wu, D.

Journal: American journal of human genetics

Citation: E. Morton, N. et D. Wu,, Alternative Bioassays of Kinship between Loci, American journal of human genetics , 42(1), 1988, pp. 173-177

Gm typing by immunoglobulin heavy-chain gene RFLP analysis

Authors: Jazwinska, E. C. Dunckley, H. Propert, D. N. Gatenby, P. A. Serjeantson, S. W.

Journal: American journal of human genetics

Citation: C. Jazwinska, E. et al., Gm typing by immunoglobulin heavy-chain gene RFLP analysis, American journal of human genetics , 43-I(2), 1988, pp. 175-181

A DNA test for indiana/swiss hereditary amyloidosis (FAP II)

Authors: Wallace, Margaret R. Conneally, P. Michael Benson, Merrill D.

Journal: American journal of human genetics

Citation: R. Wallace, Margaret et al., A DNA test for indiana/swiss hereditary amyloidosis (FAP II), American journal of human genetics , 43-I(2), 1988, pp. 182-187

Consanguineous marriage and reproduction in beirut, lebanon

Authors: Khlat, Myriam

Journal: American journal of human genetics

Citation: Khlat, Myriam, Consanguineous marriage and reproduction in beirut, lebanon, American journal of human genetics , 43-I(2), 1988, pp. 188-196

An expository review of two methods of calculating the paternity probability

Authors: Li, C. C. Chakravarti, A.

Journal: American journal of human genetics

Citation: C. Li, C. et A. Chakravarti,, An expository review of two methods of calculating the paternity probability, American journal of human genetics , 43-I(2), 1988, pp. 197-205

Uniparental disomy as a mechanism for human genetic disease

Authors: Spence, Edward Perciaccante, Ronald G. Greig, Gillian M. Willard, Huntington F. Ledbetter, David H. Heitmancik, J. Fielding Pollack, Marilyn S. O'Brien, William E. Beaudet, Arthur L.

Journal: American journal of human genetics

Citation: Spence, Edward et al., Uniparental disomy as a mechanism for human genetic disease, American journal of human genetics , 42(2), 1988, pp. 217-226

Trisomy 21 (down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21

Authors: Stewart, Gordon D. Hassold, Terry J. Berg, Andrew Watkins, Paul Tanzi, Rudolph Kurnit, David M.

Journal: American journal of human genetics

Citation: D. Stewart, Gordon et al., Trisomy 21 (down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21, American journal of human genetics , 42(2), 1988, pp. 227-236

Role of genetic polymorphism of human plasma paraoxonase/arylesterase in hydrolysis of the insecticide metabolites chlorpyrifos oxon and paraoxon

Authors: Furlong, Clement E. Richter, Rebecca J. Seidel, Sharon L. Motulsky, Arno G.

Journal: American journal of human genetics

Citation: E. Furlong, Clement et al., Role of genetic polymorphism of human plasma paraoxonase/arylesterase in hydrolysis of the insecticide metabolites chlorpyrifos oxon and paraoxon, American journal of human genetics , 43-I(3), 1988, pp. 230-238

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