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1. |
Polymorphism of Red Cell S-Formylglutathione Hydrolase in a Finnish Population |
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Human Heredity,
Volume 34,
Issue 5,
1984,
Page 273-277
Lasse Uotila,
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摘要:
Red cell hemolysates from a Finnish population sample (n = 242) were fractionated by isoelectric focusing on polyacrylamide gel, and S-formylglutathione hydrolase (EC 3.1.2.12) was located by activity staining. Polymorphism, which is probably genetically determined, was found. The samples from most persons studied gave one major enzyme band, whereas for 6 persons three enzyme bands were found. The enzyme is a dimer, and the polymorphism observed appears to result from two alleles, FGH1 and FGH2 at an autosomal locus. The frequency found for FGH1 was 0.988.
ISSN:0001-5652
DOI:10.1159/000153479
出版商:S. Karger AG
年代:1984
数据来源: Karger
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2. |
Commingling in the Distributions of Fat-Related Measures in Punjabi Families |
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Human Heredity,
Volume 34,
Issue 5,
1984,
Page 278-284
K. Sharma,
P.J. Byard,
D.C. Rao,
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摘要:
The distribution of anthropometric measurements related to fatness levels is examined to determine if skewness alone accounts for the nonnormality of such measures. A mixture of two normal distributions or a single skewed distribution fit the data significantly better than a single normal in all cases. For maximum hip width, knee diameter, and weight, two skewed distributions give a better fit than one skewed distribution, rejecting the null hypothesis of a single distribution even when skewness is considered. There is evidence for three skewed component distributions for biceps skinfold. Abdomen circumference, upper arm circumference, triceps skinfold, and calf skinfold are best approximated by a one component log-normal distribution. Children and parents show slightly different patterns in skewness and kurtosis when considered separately, but differences between them do not account for the commingling found in the combined distributions.
ISSN:0001-5652
DOI:10.1159/000153480
出版商:S. Karger AG
年代:1984
数据来源: Karger
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3. |
Quantitative and Genetic Features of Epidermal Ridge Minutiae on the Palm of Twins |
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Human Heredity,
Volume 34,
Issue 5,
1984,
Page 285-290
M. Okajima,
K. Usukura,
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摘要:
The total minutia count (TMC) and fork index (FI), i.e., the proportion of forks in total minutiae, were examined in palm prints of 20 pairs each of monozygotic and dizygotic Japanese twins. No bilateral difference was found in either trait. The mean of the TMC was higher in males than in females, but the FI showed no sex difference. Both traits presented relatively high intraclass correlation coefficients between monozygotic twins, and genetic control of these traits is suggested. However, no correlation was observed between these two traits. A slight correlation was observed between the TMC and the total palmar interdigital ridge count. Some methodological problems concerned with classification criteria were discussed.
ISSN:0001-5652
DOI:10.1159/000153481
出版商:S. Karger AG
年代:1984
数据来源: Karger
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4. |
HLA Antigens in Patients with and without a Family History of Schizophrenia |
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Human Heredity,
Volume 34,
Issue 5,
1984,
Page 291-296
Christina Rudduck,
Göran Franzén,
Bengt Löw,
Birgitta Rorsman,
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摘要:
Frequencies of HLA antigens (A, B, C and DR) were studied in patients with (n = 49) and without (n = 67) a family history of schizophrenia and in controls. Among the patients with a family history of schizophrenia significant increases were found in the A3 and B5 antigens while significant decreases were observed for the A1, A11 and B8 antigens. In a material of schizophrenic siblings the sharing of HLA haplotypes was consistent with normal segregation.
ISSN:0001-5652
DOI:10.1159/000153482
出版商:S. Karger AG
年代:1984
数据来源: Karger
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5. |
Genetic Variants of Human B Component (BF System) and Alpha-1-Antitrypsin (PI System) in a Population from Sardinia |
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Human Heredity,
Volume 34,
Issue 5,
1984,
Page 297-302
C. Davrinche,
R. Charlionet,
C. Rivat,
R. Sesboue,
M. Bayorek,
M. Arnone,
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摘要:
BF- and PI-type determinations have been performed in a population from Sardinia. The corresponding allele frequencies are as follows: BF*S = 0.5783, BF*F = 0.2189, BF*S07 = 0.0046, BF*F1 = 0.1982 and PI*M1= 0.5872, PI*M2 = 0.2041, PI*M3 = 0.0459, Pl*M4 = 0.0940, PI*S = 0.0619, PI*Z = 0.0046, PI*N = 0.0023. Whereas the BF system shows the originality of the Sardinian population with a very high BF*F1 allele frequency, the PI system does not reveal any characteristic features.
ISSN:0001-5652
DOI:10.1159/000153483
出版商:S. Karger AG
年代:1984
数据来源: Karger
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6. |
Genetic Polymorphisms in the Kuwaiti Arabs |
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Human Heredity,
Volume 34,
Issue 5,
1984,
Page 303-307
Kanwarjit Singh Sawhne,
Eric Sunderland,
Veronica Woolley,
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摘要:
Blood samples were collected from 162 Kuwaiti Arabs. These samples were typed for the ABO, MNSs, Rh, Kell and Duffy blood group systems, serum protein haptoglobins, the red cell isoenzymes acid phosphatase, phosphoglucomutase (locus 1), adenylate kinase, 6-phosphogluconate dehydrogenase, and the lactate and malate dehydrogenase variants. Comparisons were made with serological findings for other Arab populations in the Arabian peninsula.
ISSN:0001-5652
DOI:10.1159/000153484
出版商:S. Karger AG
年代:1984
数据来源: Karger
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7. |
Distribution of α1-Antitrypsin Variants in a US White Population |
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Human Heredity,
Volume 34,
Issue 5,
1984,
Page 308-310
D.D. Dykes,
S.A. Miller,
H.F. Polesky,
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摘要:
A white population from the State of Minnesota of primarily German and Scandinavian heritage was subtyped for α1-antitrypsin variants using isoelectric focusing. The frequencies of the genes PPM1 (0.724), PI*M2 (0.137) and PI*M3 (0.095) were consistent with those for white populations documented in the literature from Northern Europe. Other genes identified in the study were PI*F, PPI, PPP, PPS and PPZ
ISSN:0001-5652
DOI:10.1159/000153485
出版商:S. Karger AG
年代:1984
数据来源: Karger
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8. |
Haptoglobin Groups and Leukemia |
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Human Heredity,
Volume 34,
Issue 5,
1984,
Page 311-313
N. Fröhlander,
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摘要:
Haptoglobin groups were studied in 100 leukemia patients and controls. Previously reported associations with Hp1-1 and the Hp1 gene by other investigators were not confirmed. In agreement with a previous observation a significant increase of ahaptoglobinemia (Hp0) was found among the leukemia patients.
ISSN:0001-5652
DOI:10.1159/000153486
出版商:S. Karger AG
年代:1984
数据来源: Karger
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9. |
Genetic Relationship between Indian Tribes and Australian Aboriginals |
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Human Heredity,
Volume 34,
Issue 5,
1984,
Page 314-320
A.K. Roychoudhury,
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摘要:
Using gene frequency data often blood group and protein loci (A1A2BO, MNSs, Rh, P, Lu, Fy, Hp, Tf, Hbβ and Gm) the genetic relationships of three tribes, namely, the Toda, Irula, Kurumba in south India and one tribe, namely, the Veddah in Sri Lanka with the Aboriginals in Malay, New Guinea and Australia were studied by genetic distance analysis. The tribes in south India and Sri Lanka are genetically closer to one another than to the Aboriginals in southeast Asia and Oceania. Despite their morphological similarity there is no genetic evidence to suggest that the Indian tribes and Australian Aboriginals are biologically related
ISSN:0001-5652
DOI:10.1159/000153487
出版商:S. Karger AG
年代:1984
数据来源: Karger
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10. |
A Surveillance System for Metabolic Disorders in Japan |
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Human Heredity,
Volume 34,
Issue 5,
1984,
Page 321-327
Norikazu Yasuda,
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摘要:
Statistical procedures based on a Poisson hypothesis for surveying serial occurrences of incidence were developed. Three methods, the z-test, the cusum technique and the sequential test were applied in a study of a nationwide screening system on newborns for hereditary metabolic disorders in Japan. It was found that the statistical tests well detected human errors involved in data processing.
ISSN:0001-5652
DOI:10.1159/000153488
出版商:S. Karger AG
年代:1984
数据来源: Karger
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