1. |
X‐CHROMOSOMAL OCULAR ALBINISM IN A DUTCH FAMILY* |
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Annals of Human Genetics,
Volume 21,
Issue 2,
1956,
Page 101-122
P. J. WAARDENBURG,
J. BOSCH,
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摘要:
SUMMARYA large Dutch family stock withX‐chromosomal ocular albinism is recorded. The first generations have been formerly described by Engelhard as cases of hereditary nystagmus. This nystagmus was present indeed in all the males and in the only female person affected, but it proved to be a secondary one. The patients showed a kind of albinoidism of the tapetum, which was not quite devoid of pigment. It was combined with a hypoplasia of the fovea as in generalized albinism. The question is discussed whether this type of albinism is fully restricted to the eye or not. The mode of inheritance is an intermediate one. The female carriers are recognizable as heterozygotes by diascleral translucency of their irides and by irregular peripheral pigmentation of their fundi. The method of examination employed by the authors is described. Stress is laid upon the practical value of this research because it is now possible for daughters of transmitter females to obtain a scientifically justified prognosis for their eventual offsprin
ISSN:0003-4800
DOI:10.1111/j.1469-1809.1971.tb00270.x
出版商:Blackwell Publishing Ltd
年代:1956
数据来源: WILEY
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2. |
THE RELATIONSHIP BETWEEN PARENTAL AGE, BIRTH ORDER and THE SECONDARY SEX RATIO IN HUMANS* |
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Annals of Human Genetics,
Volume 21,
Issue 2,
1956,
Page 123-131
E. NOVITSKI,
L. SANDLER,
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摘要:
SUMMARYAn analysis is made of the change in secondary sex ratio in humans as the ages of the parents increase, and also as the age of the mother and birth order increases. It is shown that both age of the father and birth order are significantly correlated with this change in sex ratio, whereas the age of the mother is not. The changes with increasing birth order and with increasing age of the father are so similar when properly compared, that they appear quite likely to be caused by the same underlying factor.
ISSN:0003-4800
DOI:10.1111/j.1469-1809.1971.tb00271.x
出版商:Blackwell Publishing Ltd
年代:1956
数据来源: WILEY
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3. |
THE RETINAE OF MONOVULAR and BINOVULAR TWINS |
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Annals of Human Genetics,
Volume 21,
Issue 2,
1956,
Page 132-134
ROBERT PLATT,
RAYMOND LAWTON,
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ISSN:0003-4800
DOI:10.1111/j.1469-1809.1971.tb00272.x
出版商:Blackwell Publishing Ltd
年代:1956
数据来源: WILEY
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4. |
BLOOD GROUPS IN PERSIAN JEWS A COMPARATIVE STUDY WITH OTHER ORIENTAL JEWISH COMMUNITIES |
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Annals of Human Genetics,
Volume 21,
Issue 2,
1956,
Page 135-138
J. GUREVITCH,
E. HASSON,
E. MARGOLIS,
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摘要:
SUMMARYABO, MNandRh‐Hrblood‐group frequencies in 200 Persian Jews are reported and compared with findings in other oriental Jewish communit
ISSN:0003-4800
DOI:10.1111/j.1469-1809.1971.tb00273.x
出版商:Blackwell Publishing Ltd
年代:1956
数据来源: WILEY
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5. |
HEREDITY and RHEUMATIC FEVER |
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Annals of Human Genetics,
Volume 21,
Issue 2,
1956,
Page 139-144
A. C. STEVENSON,
E. A. CHEESEMAN,
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ISSN:0003-4800
DOI:10.1111/j.1469-1809.1971.tb00274.x
出版商:Blackwell Publishing Ltd
年代:1956
数据来源: WILEY
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6. |
EFFECT OF MIGRATION ON SOME GENETICAL CHARACTERS IN SIX ENDOGAMOUS GROUPS IN INDIA |
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Annals of Human Genetics,
Volume 21,
Issue 2,
1956,
Page 145-154
SATYAVATI M. SIRSAT,
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摘要:
SUMMARY1. Blood groupsOA1A2B, Rh,taste reaction to phenyl‐thio‐carbamide and colour blindness of the red‐green type have been investigated in six migrant endogamous groups in India. Data for blood groupMNhave been given for two of the six groups.2. Intra‐ and intergroup variations in these endogamous groups are analysed statistically.3. A comparative survey of some genetic traits between these migrant groups and the original community is given. Significance of the changes in gene frequencies in the estimation ofNis di
ISSN:0003-4800
DOI:10.1111/j.1469-1809.1971.tb00275.x
出版商:Blackwell Publishing Ltd
年代:1956
数据来源: WILEY
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7. |
COLOUR BLINDNESS and THE DUCHENNE‐TYPE MUSCULAR DYSTROPHY |
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Annals of Human Genetics,
Volume 21,
Issue 2,
1956,
Page 155-156
URSULA PHILIP,
JOHN N. WALTON,
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摘要:
SUMMARYA family is reported in which there was crossing‐over between the gene for the Duchenne‐type muscular dystrophy and that for incomplete red‐green colour blindness. The crossing‐over percentage
ISSN:0003-4800
DOI:10.1111/j.1469-1809.1971.tb00276.x
出版商:Blackwell Publishing Ltd
年代:1956
数据来源: WILEY
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8. |
COLOUR BLINDNESS and THE DUCHENNE‐TYPE MUSCULAR DYSTROPHY: WITH A NOTE ON THE ESTIMATION OF LINKAGE |
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Annals of Human Genetics,
Volume 21,
Issue 2,
1956,
Page 156-158
C. A. B. SMITH,
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ISSN:0003-4800
DOI:10.1111/j.1469-1809.1971.tb00277.x
出版商:Blackwell Publishing Ltd
年代:1956
数据来源: WILEY
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9. |
NAIL‐PATELLA SYNDROME: EVIDENCE FOR MODIFICATION BY ALLELES AT THE MAIN LOCUS |
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Annals of Human Genetics,
Volume 21,
Issue 2,
1956,
Page 159-169
J. H. RENWICK,
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摘要:
SUMMARYParent‐child correlations of approximately zero and sib‐sib correlations of approximately one‐half have beefi obtained in respect of the grade of seventy in the nail‐patella syndrome. The nail defect and the patellar size have been used as indices of severity.These findings are interpreted as evidence for the operation of a series of modifying genes at the nail‐patella locus itself and a possible method of confirming this interpretation is suggested in which use is made of the known linkage between this locus and the
ISSN:0003-4800
DOI:10.1111/j.1469-1809.1971.tb00278.x
出版商:Blackwell Publishing Ltd
年代:1956
数据来源: WILEY
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10. |
HAIR COLOUR IN THE INFANTILE FANCONI SYNDROME |
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Annals of Human Genetics,
Volume 21,
Issue 2,
1956,
Page 170-176
VALERIE COWIE,
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ISSN:0003-4800
DOI:10.1111/j.1469-1809.1971.tb00279.x
出版商:Blackwell Publishing Ltd
年代:1956
数据来源: WILEY
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