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1. |
No Close Linkage between MNSs and the Red Cell Acid Phosphatase |
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Human Heredity,
Volume 26,
Issue 1,
1976,
Page 1-3
Wolfgang R. Mayr,
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摘要:
A family analysis using lod scores indicates no close linkage between MNSs and the red cell acid phosphatase.
ISSN:0001-5652
DOI:10.1159/000152776
出版商:S. Karger AG
年代:1976
数据来源: Karger
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2. |
Superoxide Dismutase Variants in Newfoundland – a Gene from Scandinavia? |
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Human Heredity,
Volume 26,
Issue 1,
1976,
Page 4-7
N.D. Carter,
J.A. Auton,
S.G. Welch,
W.H. Marshall,
G.R. Fraser,
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PDF (345KB)
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摘要:
An electrophoretic survey of variant red cell enzyme phenotypes in an isolated community in Newfoundland gave gene frequencies in marked contrast to those found in the capital, St. John’s. In particular, a variant of red cell superoxide dismutase (SOD) gave a high variant frequency. Possible origins of the variant SOD allele are discusse
ISSN:0001-5652
DOI:10.1159/000152777
出版商:S. Karger AG
年代:1976
数据来源: Karger
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3. |
On the Genetics and Population Genetics of Gm(4) |
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Human Heredity,
Volume 26,
Issue 1,
1976,
Page 8-15
K.-B. Henneberg,
H. Walter,
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PDF (778KB)
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摘要:
Investigations on 70 German families with 142 children confirmed the autosomal-dominant inheritance of Gm(4). However, in our material as well as in the materials published so far, Gm(4) × Gm(–4) parental combinations show clear surplusses of Gm(4) and deficits of Gm(–4) children, which might indicate prenatal selection. The world distribution of Got4 alleles reveals a remarkable racial heterogeneity. Furthermore, marked North-South distribution gradients in Caucasoids and Mongoloids were found. The gene-tical and population genetical observations are discu
ISSN:0001-5652
DOI:10.1159/000152778
出版商:S. Karger AG
年代:1976
数据来源: Karger
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4. |
Studies of Haptoglobin and Transferrin Types in Four Castes of the Panjab, Northern India |
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Human Heredity,
Volume 26,
Issue 1,
1976,
Page 16-24
E. Sunderland,
K.S. Sawhney,
R.A. Cartwright,
J.G. Jolly,
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PDF (783KB)
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摘要:
Serum samples from 197 individuals belonging to the caste groups of Brahmin (37), Bania (39), Khatri (73) and Jat (48) were electrophoretically examined for the haptoglobin and transferrin systems. Intercaste variation was considered and comparisons made between these North Indian populations and those in other parts of the Indian subcontinent. A single Khatri individual was typed CB.
ISSN:0001-5652
DOI:10.1159/000152779
出版商:S. Karger AG
年代:1976
数据来源: Karger
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5. |
On the Geographical Variability of the red cell PGM1and Acid Phosphatase Gene Frequencies |
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Human Heredity,
Volume 26,
Issue 1,
1976,
Page 25-33
H. Walter,
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摘要:
Based on the hitherto published population data of the human red cell PGM1 and acid phosphatase polymorphisms, the geographical distributions of their gene frequencies were analyzed. As far as the acid phosphatase alleles are concerned, a marked geographical gradient was found as the Pa and Pb alleles showed significant correlations with the mean annual temperatures of the various human biotopes (Pa:r = –0.706; Pb:r = +0.812). Against that, the world distribution of the PGM1 alleles did not show a comparable correlation (PGM11:r = +0.063; PGM21:r = –0.063). The possible reasons for the distribution pattern of the acid phosphatase alleles are discus
ISSN:0001-5652
DOI:10.1159/000152780
出版商:S. Karger AG
年代:1976
数据来源: Karger
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6. |
Blood and Serum Protein Groups of the Dama of South-West Africa |
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Human Heredity,
Volume 26,
Issue 1,
1976,
Page 34-42
Rainer Knussmann,
Renate Knussmann,
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摘要:
The phenotype and gene frequencies of the following polymorphisms are given for the blood samples taken from 448 adults of the South-West African Dama Negro tribe: ABO (with sub-groups), MN, Rh, K, Hp, Gc, Gm(l,2, b), lnV(l). The frequencies are discussed in comparison with other African samples and a multivariate comparison between series from south-western Africa is conducted. The Dama prove to be relatively independent.
ISSN:0001-5652
DOI:10.1159/000152781
出版商:S. Karger AG
年代:1976
数据来源: Karger
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7. |
Human Red Cell Acid Phosphatase: Quantitative Evidence of a Silent Gene P°, and a Danish Population Study |
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Human Heredity,
Volume 26,
Issue 1,
1976,
Page 43-58
J. Dissing,
O. Svensmark,
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PDF (1559KB)
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摘要:
In a forensic case of disputed paternity an apparent mother/child incompatibility with respect to red cell acid phosphatase was found, the mother appearing as type A and the child as type B. Determination of electrophoretic type and of acid phosphatase activity in 8 of the family members strongly suggested the presence of a silent gene P° in 4 of the individuals. The phosphatase levels in the four heterozygotes were about half the values expected from normal values determined in 100 healthy adults representing the different phenotypes. The distribution of red cell acid phosphatase types in 3,735 unrelated Danish adults and in 1,109 mother/child pairs is reported; gene frequencies Pa = 0.369, Pb = 0.566 and Pc = 0.065. The P° gene frequency was roughly estimated as 0.001. Results are reported on the application of the red cell acid phosphatase system to 300 2-men cases of disputed paternit
ISSN:0001-5652
DOI:10.1159/000152782
出版商:S. Karger AG
年代:1976
数据来源: Karger
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8. |
Pancreatic Amylase Polymorphism: Another Example of a Distinctive Gene Frequency among Sardinians |
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Human Heredity,
Volume 26,
Issue 1,
1976,
Page 59-65
M. Carfagna,
L. Gaudio,
M.R. Patricolo,
F. Spadacenta,
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摘要:
The authors investigate the distribution of electrophoretic patterns of pancreatic amylase in 319 Sardinians and in 476 blood donors living in Naples. The results obtained show a difference in the phenotype frequency of the Amy2 duplication variant between Sardinians (1.25%) and Neapolitans (5.25%) which is statistically significant (p < 0.01). This further confirms that Sardinians show peculiar ethnic characteristics as compared to other Caucasian groups, even to those living in the Mediterranean area.
ISSN:0001-5652
DOI:10.1159/000152783
出版商:S. Karger AG
年代:1976
数据来源: Karger
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9. |
The G Syndrome |
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Human Heredity,
Volume 26,
Issue 1,
1976,
Page 66-71
Inger Leer Pedersen,
Margareta Mikkelsen,
Jakob Øster,
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摘要:
A male infant with hypertelorism, hypospadias, swallowing difficulties with tendency to regurgitation and cough, high arched palate, and a delicate voice, consistent with the G syndrome, is reported. In the family the same symptoms in addition to cleft lip and palate were known in several family members through four generations. In the females only slight manifestations of the syndrome were found, and in the males variable expression of symptoms was observed. Autosomal dominant inheritance is likely, but X-linked inheritance cannot be ruled out.
ISSN:0001-5652
DOI:10.1159/000152784
出版商:S. Karger AG
年代:1976
数据来源: Karger
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10. |
α-Fetoprotein Concentration in Cord Blood from Twins and from a Set of Quadruplets – a Case of Superfetatio? |
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Human Heredity,
Volume 26,
Issue 1,
1976,
Page 72-80
B. Nørgaard-Pedersen,
J. Møller,
D. Trolle,
S.A. Sørensen,
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摘要:
α-Fetoprotein has been determined in cord blood from mono- and dizygotic twins and in a case of quadruplets. The possibility of superfetatio has been evaluated by the clinically calculated gestational ages and by the α-fetoprotein levels in cord blood, especially in a case of quadruplet
ISSN:0001-5652
DOI:10.1159/000152785
出版商:S. Karger AG
年代:1976
数据来源: Karger
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