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Discrimination of Human Placental Alkaline Phosphatase Allelic Variants by Monoclonal Antibodies

Authors: Slunghter, C. A. Gogolin, K. J. Coseo, M. C. Meyer, L. J. Lesko, J. Harris, H.

Journal: American journal of human genetics

Citation: A. Slunghter, C. et al., Discrimination of Human Placental Alkaline Phosphatase Allelic Variants by Monoclonal Antibodies, American journal of human genetics , 35(1), 1983, pp. 1-20

Genetic Heterogeneity in Acid alpha-Glucosidase Deciency

Authors: Beratis, N. G. , LaBadie, G. U. and Hirschhorn, K.

Journal: American journal of human genetics

Citation: K. Beratis, N. G. , Labadie, G. U. And Hirschhorn,, Genetic Heterogeneity in Acid alpha-Glucosidase Deciency, American journal of human genetics , 35(1), 1983, pp. 21-33

A Sib-Pair Strategy for the Use of Restriction Fragment Lenght Polymorphisms to Study the Mode of Transmission of Type II Diabetes

Authors: Suarez, B K.

Journal: American journal of human genetics

Citation: K. Suarez, B, A Sib-Pair Strategy for the Use of Restriction Fragment Lenght Polymorphisms to Study the Mode of Transmission of Type II Diabetes, American journal of human genetics , 35(1), 1983, pp. 34-48

Detection of Genetic Variation with Radioactive Ligands. V. Genetic Variants of Testosterone-Binding Globulin in Human Serum

Authors: Luckock, A. and Cavalli-Sforza, L. L.

Journal: American journal of human genetics

Citation: L. Luckock, A. And Cavalli-sforza, L., Detection of Genetic Variation with Radioactive Ligands. V. Genetic Variants of Testosterone-Binding Globulin in Human Serum, American journal of human genetics , 35(1), 1983, pp. 49-57

Studies on the Radiosensitivity of Cells from Patients with Basal Cell Naevus Syndrome

Authors: Featherstone, T. , Taylor, A. M. R. and Harnden, D. G.

Journal: American journal of human genetics

Citation: G. Featherstone, T. , Taylor, A. M. R. And Harnden, D., Studies on the Radiosensitivity of Cells from Patients with Basal Cell Naevus Syndrome, American journal of human genetics , 35(1), 1983, pp. 58-66

Gastrict Juice in Congenital Pernicious Anemia Contains No Immunoreactive Intrinsic Factor Molecule: Study of Three Kindreds with Variable Ages at Presentation, Including a Patient First Diagnosed in Adullthood

Authors: Carmel, R.

Journal: American journal of human genetics

Citation: R. Carmel,, Gastrict Juice in Congenital Pernicious Anemia Contains No Immunoreactive Intrinsic Factor Molecule: Study of Three Kindreds with Variable Ages at Presentation, Including a Patient First Diagnosed in Adullthood, American journal of human genetics , 35(1), 1983, pp. 67-77

Linkage of Atypical Vitelliform Macular Dystrophy (VDM-1) to the Soluble Glutamate Pyruvate Transaminase (GPT1) Locus

Authors: Ferrell, R. E. , Hittner, H. M. and Antoszyk, J. H.

Journal: American journal of human genetics

Citation: H. Ferrell, R. E. , Hittner, H. M. And Antoszyk, J., Linkage of Atypical Vitelliform Macular Dystrophy (VDM-1) to the Soluble Glutamate Pyruvate Transaminase (GPT1) Locus, American journal of human genetics , 35(1), 1983, pp. 78-84

Citrullinemia: Prenatal Diagnosis of an Affected Fetus

Authors: Fleisher, L. D. , Harris, C. J. , Mitchell, D. A. and Nadler, H. L.

Journal: American journal of human genetics

Citation: L. Fleisher, L. D. , Harris, C. J. , Mitchell, D. A. And Nadler, H., Citrullinemia: Prenatal Diagnosis of an Affected Fetus, American journal of human genetics , 35(1), 1983, pp. 85-90

Terminal Deletion with Stable Acentric Fragment of 1q in a Child with Congenital Malformations

Authors: Kucerovà, M. , Polivkovà, Z. , Dluholucky, S. and Kvasnicovà, M.

Journal: American journal of human genetics

Citation: M. Kucerovà, M. , Polivkovà, Z. , Dluholucky, S. And Kvasnicovà,, Terminal Deletion with Stable Acentric Fragment of 1q in a Child with Congenital Malformations, American journal of human genetics , 35(1), 1983, pp. 91-95

Rates of Mutant Structural Chromosome Rearrangements in Human Fetuses: Data from Prenatal Cytogenetic Studies and Associations with Maternal Age and Parental Mutagen Exposure

Authors: Hook, E. B. , Schreinemachers, D. M: , Willey, A. M. and Cross, P. K.

Journal: American journal of human genetics

Citation: K. Hook, E. B. , Schreinemachers, D. M: , Willey, A. M. And Cross, P., Rates of Mutant Structural Chromosome Rearrangements in Human Fetuses: Data from Prenatal Cytogenetic Studies and Associations with Maternal Age and Parental Mutagen Exposure, American journal of human genetics , 35(1), 1983, pp. 96-109

Chromosome Abnormalities and Spontaneous Fetal Death following Amniocentesis: Further Data and Associations with Maternal Age

Authors: Hook, E. B.

Journal: American journal of human genetics

Citation: B. Hook, E., Chromosome Abnormalities and Spontaneous Fetal Death following Amniocentesis: Further Data and Associations with Maternal Age, American journal of human genetics , 35(1), 1983, pp. 110-116

The Combined Effects of FUdR Addition and Methionine Depletion on the X-Chromosome Fragile Site

Authors: Glover, T. W. and Howard-Peebles, P. N.

Journal: American journal of human genetics

Citation: N. Glover, T. W. And Howard-peebles, P., The Combined Effects of FUdR Addition and Methionine Depletion on the X-Chromosome Fragile Site, American journal of human genetics , 35(1), 1983, pp. 117-122

Spontaneous Expression of the Chromosome Fragile Sita fra(10)(q25)

Authors: Taylor, A. M. R. and Bundey, S.

Journal: American journal of human genetics

Citation: S. Taylor, A. M. R. And Bundey,, Spontaneous Expression of the Chromosome Fragile Sita fra(10)(q25), American journal of human genetics , 35(1), 1983, pp. 123-125

Expression of Fragile Sites at 10q25 in Normal Culture Conditions

Authors: Petit, P. and Fryns, J. P.

Journal: American journal of human genetics

Citation: P. Petit, P. And Fryns, J., Expression of Fragile Sites at 10q25 in Normal Culture Conditions, American journal of human genetics , 35(1), 1983, pp. 126-126

A New Methodology for Analysis of HLA-Associated Disease?

Authors: Clerget-Darpoux, F. Goldin, L. R. and Gershon, E. S.

Journal: American journal of human genetics

Citation: S. Clerget-darpoux, F. Goldin, L. R. And Gershon, E., A New Methodology for Analysis of HLA-Associated Disease?, American journal of human genetics , 35(1), 1983, pp. 127-129

Genetic Analysis of Multifactorial Disease

Authors: Weitkamp, Lowell R.

Journal: American journal of human genetics

Citation: R. Weitkamp, Lowell, Genetic Analysis of Multifactorial Disease, American journal of human genetics , 35(1), 1983, pp. 130-133

Amino Acid Change Associated with the Major Polymorphic Hinc II Site of Oriental and Caucasian Mitochondrial DNA's

Authors: Blanc, H. , Chen, K. -H. , D'Amore, M. A. and Wallace, D. C.

Journal: American journal of human genetics

Citation: C. Blanc, H. , Chen, K. -h. , D'Amore, M. A. And Wallace, D., Amino Acid Change Associated with the Major Polymorphic Hinc II Site of Oriental and Caucasian Mitochondrial DNA's, American journal of human genetics , 35(2), 1983, pp. 167-176

Some Combinatorial Problems of DNA Restriction Fragment Lenght Polymorphisms

Authors: Lange, K. and Boehnke, M.

Journal: American journal of human genetics

Citation: M. Lange, K. And Boehnke,, Some Combinatorial Problems of DNA Restriction Fragment Lenght Polymorphisms, American journal of human genetics , 35(2), 1983, pp. 177-192

Polymorphism in the 5'-Flanking Region of the Human Insulin Gene and the Incidence of Diabetes

Authors: Yokoyama, S.

Journal: American journal of human genetics

Citation: S. Yokoyama,, Polymorphism in the 5'-Flanking Region of the Human Insulin Gene and the Incidence of Diabetes, American journal of human genetics , 35(2), 1983, pp. 193-200

Heterozygous Expression of Insuline-Dependent Diabetes Mellitus (IDDM) Determinants in the HLA System

Authors: Morton, N. E. , Green, A. , Dunsworth, T. , Svejgaard, A. , Barbosa, J. , Rich S

Journal: American journal of human genetics

Citation: S. Morton, N. E. , Green, A. , Dunsworth, T. , Svejgaard, A. , Barbosa, J. , Rich, Heterozygous Expression of Insuline-Dependent Diabetes Mellitus (IDDM) Determinants in the HLA System, American journal of human genetics , 35(2), 1983, pp. 201-213

The Human Serum Paraoxonase Polymorphism: Identification of Phenotypes by Their Response to Salts

Authors: Eckerson, H. W. , Romson, J. , Wyte, C. and La Du, B. N.

Journal: American journal of human genetics

Citation: N. Eckerson, H. W. , Romson, J. , Wyte, C. And La Du, B., The Human Serum Paraoxonase Polymorphism: Identification of Phenotypes by Their Response to Salts, American journal of human genetics , 35(2), 1983, pp. 214-227

Two Allelic forms of human arylsulfatase A with different numbers of Asparagine-linked oligosaccharides

Authors: Waheed, A. , Steckel, F. , Hasilik, A. and von Figura, K.

Journal: American journal of human genetics

Citation: K. Waheed, A. , Steckel, F. , Hasilik, A. And Von Figura,, Two Allelic forms of human arylsulfatase A with different numbers of Asparagine-linked oligosaccharides, American journal of human genetics , 35(2), 1983, pp. 228-233

Evidence for a dosage effect at the X-Linked steroid sulfatase locus in human tissues

Authors: Chance, P. F. and Gartler, S. M.

Journal: American journal of human genetics

Citation: M. Chance, P. F. And Gartler, S., Evidence for a dosage effect at the X-Linked steroid sulfatase locus in human tissues, American journal of human genetics , 35(2), 1983, pp. 234-240

Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistyping

Authors: Lathrop, G. M. , Hooper, A. B. , Huntsman, J. W. and Ward, R. H.

Journal: American journal of human genetics

Citation: H. Lathrop, G. M. , Hooper, A. B. , Huntsman, J. W. And Ward, R., Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistyping, American journal of human genetics , 35(2), 1983, pp. 241-262

Linkage between a marker locus and a quantitative trait of sibs

Authors: Cockerham, C. C: and Weir, B. S.

Journal: American journal of human genetics

Citation: S. Cockerham, C. C: And Weir, B., Linkage between a marker locus and a quantitative trait of sibs, American journal of human genetics , 35(2), 1983, pp. 263-273

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