Selective abortion, gametic selection, and the X chromosome.
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Abortion, Therapeutic↗
Biomedical subjects
G R Fraser
Publications and source records attributed to G R Fraser.
Genetical influences on serum--cholesterol level.
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ABO Blood-Group System↗
Congenital internal carotid--internal jugular fistula.
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Arteriovenous Fistula↗
Genetic approaches to the nosology of deafness.
Profound deafness of childhood is a heterogeneous entity. Perhaps 50% of cases owe their handicap to mendelian segregation of single genes. Various types of genetic methods, combined with clinical and statistical analyses, are described by means of which an initial approach can be made to the problem of the estimation of the number of different gene loci involved and of the prevalence of the various abnormal alleles, as well as of the definition of their modes of action.
Alleles↗
The genetics of congenital deafness.
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Abnormalities, Multiple↗
Public health and long-term genetic implications of intrauterine diagnosis and selective abortion.
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Abortion, Therapeutic↗
The handless and footless families of Brazil.
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Abnormalities, Multiple↗
Clonal origin for individual Burkitt tumours.
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Burkitt Lymphoma↗
The causes of profound deafness in childhood. In: Sensorinerual hearing loss.
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Abnormalities, Multiple↗
Karyotype studies among children with severe visual handicap.
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Adolescent↗
Genetical aspects of severe visual impairment in childhood.
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Anophthalmos↗
Association of juvenile diabetes mellitus, primary optic atrophy and perceptive hearing loss in three sibs, with additional idiopathic diabetes mellitus insipidus in one case.
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Adolescent↗
The linkage between protan and deutan loci.
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Color Vision Defects↗
Dysplasia spondyloepiphysaria congenita and related generalized skeletal dysplasias among children with severe visual handicaps.
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Adolescent↗
Serum polymorphisms in Yugoslavia.
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Blood Proteins↗
Genetic influences on serum cholesterol in two Greek villages.
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Adolescent↗
Gene frequencies at loci determining blood-group and serum-protein polymorphisms in two villages of northwestern Greece.
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ABO Blood-Group System↗
The genetics of thyroid disease.
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Chromosome Aberrations↗