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1. |
The Effects of Parental Consanguinity and Inbreeding in Hirado, Japan III. Vision and Hearing |
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Human Heredity,
Volume 20,
Issue 2,
1970,
Page 129-155
J.V. Neel,
W.J. Schull,
T. Kimura,
Y. Tanigawa,
M. Yamamoto,
A. Nakajima,
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摘要:
The effects of parental consanguinity, age, and sex on defects of the eye and ear, accomodation, mean visual acuity, and mean decibels of hearing loss at four frequencies have been investigated in a series of Middle School children and their parents on Hirado Island, Japan. In the children the effect of paternal and maternal inbreeding on these same indicators has also been investigated. The numbers available for the various analyses after eliminations for incompleteness of records, and confining the analysis to children where socioeconomic data are complete, are given in table III. Age and sex effects are encountered at high levels of statistical significance, but, unlike the results on Hirado with respect to a variety of other indicators [Schull et al., 1970; Neel et al., 1970], socioeconomic effects are negligible. None of the regressions on consanguinity or inbreeding is individually significant, nor is there any consistent pattern to the totality of the regressions. On the other hand, the sampling errors are such that the data cannot be said to conflict with the significant positive findings regarding consanguinity effects in a previous study in Hiroshima and Nagasaki [Schull and Neel, 1965].
ISSN:0001-5652
DOI:10.1159/000152303
出版商:S. Karger AG
年代:1970
数据来源: Karger
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2. |
The Genetical Interpretation of Haemoglobin H Disease |
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Human Heredity,
Volume 20,
Issue 2,
1970,
Page 156-164
C. Kattamis,
H. Lehmann,
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摘要:
The clinical and haematological data of nine patients with haemoglobin H disease, as well as of 16 members of their families, are reported. Pedigree study and haematological data permit the assumption that in an individual four genes could be responsible for α-chain synthesis. Based on this hypothesis, four variants of α-thalassaemia are expected to exist. The first, in which only one gene is affected has no, or only minor, red cell changes and an increase in Hb Bart’s at birth, the second with two genes affected has in addition Hb H inclusion bodies in a few red cells, the third, with three genes affected represents haemoglobin H disease, and the fourth, with all four genes affected, represents homozygous α-thalassaemia, which is incompatible with life and results in a stillborn child with hydrops foet
ISSN:0001-5652
DOI:10.1159/000152304
出版商:S. Karger AG
年代:1970
数据来源: Karger
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3. |
Model Estimates of the Number of Gene Pairs Involved in Pigmentation Variability of the Negro-American |
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Human Heredity,
Volume 20,
Issue 2,
1970,
Page 165-168
C. Stern,
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摘要:
This note presents revised model derivations for pigmentation distributions in the Negro-American. Instead of the formerly accepted estimate of 30% Caucasian alleles the recent estimate of 20% has been used. Best agreement with observations is obtained from 3 and 4 pair models. The uncertainties of the treatment are emphasized.
ISSN:0001-5652
DOI:10.1159/000152305
出版商:S. Karger AG
年代:1970
数据来源: Karger
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4. |
Population Structure of A, B, O, AB Blood Groups in Belgium |
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Human Heredity,
Volume 20,
Issue 2,
1970,
Page 169-177
P.A. Dodinval,
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摘要:
The theory of Malecot about the decrease of kinship with distance was tested with a big material of ABO blood groups distributed all over Belgium. The kinship, calculated from the frequency of random pairs of blood groups decreases exponentially with a good fit to the theory. Subdivisions of Belgium are also studied in the same way and differences between regions according to inbreeding and distances between mates are discussed.
ISSN:0001-5652
DOI:10.1159/000152306
出版商:S. Karger AG
年代:1970
数据来源: Karger
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5. |
Human Erythrocyte Adenosine Deaminase Polymorphism in Denmark |
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Human Heredity,
Volume 20,
Issue 2,
1970,
Page 178-181
J. Dissing,
J.B. Knudsen,
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摘要:
The ADA types of human red cells are reported for a material of 1321 unrelated adults in Denmark. The gene frequencies observed are: ADA1 = 0.9391 and ADA2 = 0.0609. The study of 754 mother-child pairs provides further evidence for a simple Mendelian codominant way of inheritance.
ISSN:0001-5652
DOI:10.1159/000152307
出版商:S. Karger AG
年代:1970
数据来源: Karger
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6. |
Isozyme Variations in Human Cells Grownin vitroIV. Identity between Alkaline Phosphatases from HeLa Cells and Placenta? |
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Human Heredity,
Volume 20,
Issue 2,
1970,
Page 182-186
G. Beckman,
L. Beckman,
E. Lundgren,
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摘要:
Evidence is presented suggesting that the heat-stable alkaline phosphatase of HeLa cells is identical with a specific genetic variant (Sx) of placental alkaline phosphatase.
ISSN:0001-5652
DOI:10.1159/000152308
出版商:S. Karger AG
年代:1970
数据来源: Karger
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7. |
Relation between the ABO Blood Groups and the Level of Placental Alkaline Phosphatase in Sera of Pregnant Women |
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Human Heredity,
Volume 20,
Issue 2,
1970,
Page 187-192
G. Beckman,
L. Beckman,
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摘要:
The relation between the ABO blood groups and the serum level of the heat-stable placental alkaline phosphatase was studied in a series of about 400 pregnant women. The claim by other investigators that significantly lower enzyme levels are found in mothers of blood group 0 could not be confirmed in this investigation. No association was found between the ABO blood groups and the heat-sensitive (liver) alkaline phosphatase. Thus conclusive evidence for a blood group association has so far been established for intestinal alkaline phosphatase only.
ISSN:0001-5652
DOI:10.1159/000152309
出版商:S. Karger AG
年代:1970
数据来源: Karger
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8. |
Distribution of Placental Alkaline Phosphatase Types in a Japanese Population |
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Human Heredity,
Volume 20,
Issue 2,
1970,
Page 193-198
G. Ishimoto,
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摘要:
The placental alkaline phosphatase types have been determined in a series of 374 Japanese placentae. Nine different phenotypes were observed, and the gene frequencies for the common phenotypes are calculated Pls1 = 0.721, Pli1 = 0.225 and Plf1 = 0.043. In contrast to reports on Caucasians, the high Pli1 and the low Plf1 are characteristic of the present study. Rare alleles probably corresponding to Pls2 and Pls3 are also present and a new phenotype tentatively designated S1SJ is described.
ISSN:0001-5652
DOI:10.1159/000152310
出版商:S. Karger AG
年代:1970
数据来源: Karger
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9. |
Red Cell Acid Phosphatase Types in Poland Population and Genetic Studies |
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Human Heredity,
Volume 20,
Issue 2,
1970,
Page 199-208
Barbara Wyslouchowa,
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摘要:
Phenotype- and gene-frequencies of red cell acid phosphatase in the Polish population have been determined. Analysis of a family material supports the genetic hypothesis that the acid phophatase is controlled by three codominant allelic genes. The utility of determination of acid phosphatase types in twin studies, paternity testing and in anthropological investigations is discussed.
ISSN:0001-5652
DOI:10.1159/000152311
出版商:S. Karger AG
年代:1970
数据来源: Karger
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10. |
The Haptoglobin and Transferrin Types in West Bengal and a Case of Haptoglobin ‘Johnson’ |
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Human Heredity,
Volume 20,
Issue 2,
1970,
Page 209-214
B.N. Mukherjee,
S.K. Das,
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摘要:
A series of 456 serum samples obtained from blood donors in Central Blood Bank, Calcutta, were examined by starch gel electrophoresis for haptoglobin types, and 424 samples out of them were examined for transferrin types. Hp1 gene-frequency was 0.16, and the HpO frequency just under 1%. The first case of Hp ‘Johnson’ in India was detected in a Bengali Hindu. No transferrin variants were detected, all being of the common CC t
ISSN:0001-5652
DOI:10.1159/000152312
出版商:S. Karger AG
年代:1970
数据来源: Karger
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