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Articles table of contents

Results : 26-50/117

DNA Restriction Fragment Analysis of the Proopiomelanocortin Gene in Schizophrenia and Bipolar Disorders.

Authors: Feder, J. , Gurling, H. M. D. , Darby, J. and Cavalli-Sforza, L. L.

Journal: American journal of human genetics

Citation: L. Feder, J. , Gurling, H. M. D. , Darby, J. And Cavalli-sforza, L., DNA Restriction Fragment Analysis of the Proopiomelanocortin Gene in Schizophrenia and Bipolar Disorders., American journal of human genetics , 37(2), 1985, pp. 286-294

Transfer of Human and Murine Globin-Gene Sequences into Transgenic Mice.

Authors: Humphries, R. K. , Berg, P. , Di Pietro, J. , Bernstein, S. , Baur, A. , Nienhui

Journal: American journal of human genetics

Citation: Humphries, R. K. , Berg, P. , Di Pietro, J. , Bernstein, S. , Baur, A. , Nienhui, Transfer of Human and Murine Globin-Gene Sequences into Transgenic Mice., American journal of human genetics , 37(2), 1985, pp. 295-310

A Molecular Basis for Discrete Size Variation in Human Ribosomal DNA.

Authors: Erickson, J. M. and Schmickel, R. D.

Journal: American journal of human genetics

Citation: D. Erickson, J. M. And Schmickel, R., A Molecular Basis for Discrete Size Variation in Human Ribosomal DNA., American journal of human genetics , 37(2), 1985, pp. 311-325

Heterogeneity of Holocarboxylase Synthetase in Patients with Biotin- Responsive Multiple Carboxylase Deficiency.

Authors: Burri, B. J. , Sweetman, L. and Nyhan, W. L.

Journal: American journal of human genetics

Citation: L. Burri, B. J. , Sweetman, L. And Nyhan, W., Heterogeneity of Holocarboxylase Synthetase in Patients with Biotin- Responsive Multiple Carboxylase Deficiency., American journal of human genetics , 37(2), 1985, pp. 326-337

Incidence in Italy, Genetic Heterogeneity, and Segregation Analysis of Cystic Fibrosis.

Authors: Romeo, G. , Bianco, M. , Devoto, M. , Menozzi, P. , Mastella, G. , Giunta, A. M.

Journal: American journal of human genetics

Citation: M. Romeo, G. , Bianco, M. , Devoto, M. , Menozzi, P. , Mastella, G. , Giunta, A., Incidence in Italy, Genetic Heterogeneity, and Segregation Analysis of Cystic Fibrosis., American journal of human genetics , 37(2), 1985, pp. 338-349

A Genetic Model for Age at Onset in Huntington Disease.

Authors: Farrer, L. A. and Conneally, P. M.

Journal: American journal of human genetics

Citation: M. Farrer, L. A. And Conneally, P., A Genetic Model for Age at Onset in Huntington Disease., American journal of human genetics , 37(2), 1985, pp. 350-357

y-Aminobutyric Acid Transaminase (GABAT) Polymorphism among Ethnic Groups in Singapore- - With Report of a New Allele.

Authors: Bhattacharyya, S. P. , Saha, N. and Wee, K. P.

Journal: American journal of human genetics

Citation: P. Bhattacharyya, S. P. , Saha, N. And Wee, K., y-Aminobutyric Acid Transaminase (GABAT) Polymorphism among Ethnic Groups in Singapore- - With Report of a New Allele., American journal of human genetics , 37(2), 1985, pp. 358-361

Paternal-Age and Birth-Order Effect: The Human Secondary Sex Ratio.

Authors: Ruder, A.

Journal: American journal of human genetics

Citation: A. Ruder,, Paternal-Age and Birth-Order Effect: The Human Secondary Sex Ratio., American journal of human genetics , 37(2), 1985, pp. 362-372

Estimation of Inbreeding by Isonymy in Iberoamerican Populations: An Extension of the Method of Crow and Mange.

Authors: Pinto-Cisternas, J. , Pineda, L. and Barrai, I.

Journal: American journal of human genetics

Citation: I. Pinto-cisternas, J. , Pineda, L. And Barrai,, Estimation of Inbreeding by Isonymy in Iberoamerican Populations: An Extension of the Method of Crow and Mange., American journal of human genetics , 37(2), 1985, pp. 373-385

Bibliography of Cloned Human and Other Selected DNAs.

Authors: Beaudet, A. L.

Journal: American journal of human genetics

Citation: L. Beaudet, A., Bibliography of Cloned Human and Other Selected DNAs., American journal of human genetics , 37(2), 1985, pp. 386-406

Mapping of Rare X-Linked Becker Muscular Dystrophy through Double Crossovers Identified by DNA Polymorphisms and by Haplotype Characterization in Somatic Cell Hybrids.

Authors: Roncuzzi, L. , Fadda, S. , Mochi, M. , Prosperi, L. , Sangiorgi, S. , Santamaria

Journal: American journal of human genetics

Citation: Roncuzzi, L. , Fadda, S. , Mochi, M. , Prosperi, L. , Sangiorgi, S. , Santamaria, Mapping of Rare X-Linked Becker Muscular Dystrophy through Double Crossovers Identified by DNA Polymorphisms and by Haplotype Characterization in Somatic Cell Hybrids., American journal of human genetics , 37(2), 1985, pp. 407-417

Human Salivary Proline-Rich Protein Genes on Chromosome 12.

Authors: Azen, E. A. , Goodman, P. A. and Lalley, P. A.

Journal: American journal of human genetics

Citation: A. Azen, E. A. , Goodman, P. A. And Lalley, P., Human Salivary Proline-Rich Protein Genes on Chromosome 12., American journal of human genetics , 37(2), 1985, pp. 418-424

Anti-Kinetochore Antibodies: Use as Probes for Inactive Centromeres.

Authors: Merry, D. E. , Pathak, S. , Hsu, T. C. and Brinkley, B. R.

Journal: American journal of human genetics

Citation: R. Merry, D. E. , Pathak, S. , Hsu, T. C. And Brinkley, B., Anti-Kinetochore Antibodies: Use as Probes for Inactive Centromeres., American journal of human genetics , 37(2), 1985, pp. 425-430

Book Reviews

Authors:

Journal: American journal of human genetics

Citation: , Book Reviews, American journal of human genetics , 37(2), 1985, pp. 431-434

Tourette Syndrome: Clinical and Psychological aspects of 250 cases

Authors: Comings, D. E. , Comings, B. G.

Journal: American journal of human genetics

Citation: G. Comings, D. E. , Comings, B., Tourette Syndrome: Clinical and Psychological aspects of 250 cases, American journal of human genetics , 37(3), 1985, pp. 435-450

Mapping DNA Sequences in a Human X-Chromosome Deletion Which Extends across the Region of the Duchenne Muscular Dystrophy Mutation.

Authors: Ingle, C. , Williamson, R. , de la Chapelle, A. , Herva, R. R. , Haapala, K. , B

Journal: American journal of human genetics

Citation: B. Ingle, C. , Williamson, R. , De La Chapelle, A. , Herva, R. R. , Haapala, K. ,, Mapping DNA Sequences in a Human X-Chromosome Deletion Which Extends across the Region of the Duchenne Muscular Dystrophy Mutation., American journal of human genetics , 37(3), 1985, pp. 451-462

Genetic Mapping of DNA Segments Relative to the Locus for the Fragile-X

Authors: White, B. N.

Journal: American journal of human genetics

Citation: N. White, B., Genetic Mapping of DNA Segments Relative to the Locus for the Fragile-X, American journal of human genetics , 37(3), 1985, pp. 463-472

Choroideremia Is Linked to the Restriction Fragment Length Polymorphism DXYSI at XQ13-21.

Authors: Nussbaum, , R. L. , Lewis, R. A. , Lesko, J. G. , and Ferrell, R.

Journal: American journal of human genetics

Citation: R. Nussbaum, , R. L. , Lewis, R. A. , Lesko, J. G. , And Ferrell,, Choroideremia Is Linked to the Restriction Fragment Length Polymorphism DXYSI at XQ13-21., American journal of human genetics , 37(3), 1985, pp. 473-481

Multilocus Linkage Analysis in Humans: Detection of Linkage and Estimation of Recombination.

Authors: Lathrop, G. M. , Lalouel, J. M. , Julier, C. and Ott, J.

Journal: American journal of human genetics

Citation: J. Lathrop, G. M. , Lalouel, J. M. , Julier, C. And Ott,, Multilocus Linkage Analysis in Humans: Detection of Linkage and Estimation of Recombination., American journal of human genetics , 37(3), 1985, pp. 482-498

Gaucher Disease Types 1, 2, and 3: Differential Mutations of the Acid ß- Glucosidase Active Site Identified with Conduritol B Epoxide Derivatives and Sphingosine

Authors: Grabowski, G. A. , Dinur, T. , Osiecki, K. M. , Kruse, J. R. , Legler, G. and Ga

Journal: American journal of human genetics

Citation: Grabowski, G. A. , Dinur, T. , Osiecki, K. M. , Kruse, J. R. , Legler, G. And Ga, Gaucher Disease Types 1, 2, and 3: Differential Mutations of the Acid ß- Glucosidase Active Site Identified with Conduritol B Epoxide Derivatives and Sphingosine, American journal of human genetics , 37(3), 1985, pp. 499-510

Maternal Factors in Onset of Huntington Disease.

Authors: Myers, R. H. , Cupples, L. A., Schoenfeld, M. , D'Agostino, R. B. , Terrin, N. C

Journal: American journal of human genetics

Citation: C. Myers, R. H. , Cupples, L. A., Schoenfeld, M. , D'Agostino, R. B. , Terrin, N., Maternal Factors in Onset of Huntington Disease., American journal of human genetics , 37(3), 1985, pp. 511-523

Chromosome-Specific Organization of Human Alpha Satellite DNA.

Authors: Willard, H. F.

Journal: American journal of human genetics

Citation: F. Willard, H., Chromosome-Specific Organization of Human Alpha Satellite DNA., American journal of human genetics , 37(3), 1985, pp. 524-532

Segregation and Fertility Analysis in an Autosomal Reciprocal Translocation ((1;8) (q41;q23.1)

Authors: Vauhkonen, . A.-E. , Sankila, E.-M. , Simola, K. O. J. and de la Chapelle, A.

Journal: American journal of human genetics

Citation: A. Vauhkonen, . A.-e. , Sankila, E.-m. , Simola, K. O. J. And De La Chapelle,, Segregation and Fertility Analysis in an Autosomal Reciprocal Translocation ((1;8) (q41;q23.1), American journal of human genetics , 37(3), 1985, pp. 533-542

Folic Acid Blinded Trial in Identical Twins with Fragile X Syndrome.

Authors: Rosenblatt, D. S. , Duschenes, E. A. , Hellstrom, F. V. , Golick, M. S. , Vekema

Journal: American journal of human genetics

Citation: Rosenblatt, D. S. , Duschenes, E. A. , Hellstrom, F. V. , Golick, M. S. , Vekema, Folic Acid Blinded Trial in Identical Twins with Fragile X Syndrome., American journal of human genetics , 37(3), 1985, pp. 543-552

An Unstable Giant Satellite Associated with Chromosomes 21 and 22 in the Same Individual.

Authors: Livingston, G. K. , Lockey, J. E. , Witt, K. S. , and Rogers, S. W.

Journal: American journal of human genetics

Citation: W. Livingston, G. K. , Lockey, J. E. , Witt, K. S. , And Rogers, S., An Unstable Giant Satellite Associated with Chromosomes 21 and 22 in the Same Individual., American journal of human genetics , 37(3), 1985, pp. 553-560

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