Journal of Medical Genetics - 1971

116 articles | Last updated: 2025-12-03 14:12:57
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Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Presumptive 46,XX-46,XY-47,XXY mosaicism in a hermaphrodite.
Clinical Genetics: An International Journal of Genetics in Medicine
Medizinische Genetik. Grundlagen, Ergebnisse und Probleme
Ahaptoglobinaemia and predisposition to iron-deficiency anaemia.
Double heterozygosity for glucose-6-phosphate dehydrogenase deficiency.
Correspondence
Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance.
Distribution of ABO blood groups, G6PD deficiency, and abnormal haemoglobins in leprosy.
Rh immunization following incompatible blood transfusion and a possible long-term complication of anti-D immunoglobulin therapy.
The Post-natal Development of Phenotype
Klassische und Molekulare Genetik
Genetic Counselling
Cold Spring Harbor Symposia on Quantitative Biology, Vol. XXXV
A case of 47,XX,(21q-)+ with some stigmata of Down's syndrome and an IQ of 77.
Developmental Processes in Higher Vertebrates
Trisomy of chromosome 16 in a neonate, 47XY,?16+.
Methoden in der medizinischen Cytogenetik
The genetic basis of variation in factor 8 levels among haemophiliacs.
Genetic studies on hypospadias in males.
Virilizing adrenal carcinoma in two sibs.
Chromosomal aberrations induced by T strains mycoplasmas.
A family with balanced translocation, t(5p-;Gp+).
Ring 13 chromosome with normal haptoglobin inheritance.
The use of quinacrine fluorescence in the identification of B and E group chromosomes involved in structural abnormalities.
Epidemiology of Mongolism
An ABC of Medical Genetics
Mutation rate in Duchenne muscular dystrophy.
X chromosome long arm deletion in a patient with Down's syndrome.
Genetic Epistemology
The X-linked blood group system Xg. Tests on unrelated people and families of northern European ancestry. northern European ancestry
Polymorphism and protein evolution. The neutral mutation-random drift hypothesis.
The nosology of the spinal muscular atrophies.
Origin of sex chromosome monosomy in man.
Phenylketonuria.
Genetic control of nortriptyline kinetics in man: a study of relatives of propositi with high plasma concentrations.
Di Guglielmo syndrome in a t(DgDg) heterozygote.
Birth Defects: Original Article Series, V, 2
Familial total anomalous pulmonary venous return.
Trisomy D-trisomy E mosaicism in an infant male.
Carcinoma of the breast and Klinefelter's syndrome.
On the pathogenesis of favism.
Simple anonychia. Further evidence for autosomal recessive inheritance.
Essentials of Medical Genetics
Concordance for amyotrophic lateral sclerosis in a pair of dizygous twins of consanguineous parents.
Congenital cleft lip. A genetic study of 496 propositi.
Familial incidence of cerebrovascular disease.
Genetics of childhood spinal muscular atrophy.
47,XX,13+ with Snodgrass phenotype II. Are different chromosomes associated with two clinical varieties of D-trisomy?
Mental retardation, unusual facies, and abnormal nails associated with a group-G ring chromosome. A case report on two unrelated cases.
A group-C ring chromosome in a mentally deficient male.
A child with a ring G chromosome (46,XX, Gr).
Birth Defects: Original Article Series, V, 3
Differentiation of two genetically specific types of depression by the response to antidepressant drugs.
Suppression of the immune response.
Group G deletion syndromes.
The inheritance of a structural anomaly of one chromosome No. 16 in a kindred (46,16-,C+).
Partial deletion of a group-F (19-20) chromosome in a physically handicapped psychiatric male patient.
An extra small metacentric autosome in a mentally retarded boy with multiple malformations.
Birth Defects; Original Article Series, V. 4
Advances in Twin Studies
An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy.
Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.
-glucuronidase activity in fibroblasts cultured from persons with and without cystic fibrosis.
Individuals at risk in families with genetic disease.
Abnormal distribution of ABO blood groups in infantile pyloric stenosis.
Monosomy G: case report and review of the literature.
Autosomal translocation in a mentally retarded male child with 46,XY,t(2q-;13q+) complement. Case report and review.
A family showing transmission of a translocation t(3porq-;Cq+).
A 47,XXq-Y Klinefelter male.
Genetics of the Evolutionary Process
Asphyxiating thoracic chondrodystrophy. Association with renal disease and evidence for possile heterozygous expression.
Ovum Implantation: Its Hormonal, Biochemical, Neurophysiological and Immunological Bases
Corrigendum
An inherited kidney disease of mice resembling human nephronophthisis.
Chromosome surveys in penal institutions and approved schools.
Chromosome studies in 101 mentally handicapped Jamaican children.
Gene deletion and duplication effects on phenotype and gamma globulin levels.
A familial variant of chromosome 9.
A case of XYY Down's syndrome confirmed by autoradiography.
49,XXXXY chromossomal anomaly in a neonate.
The De Lange Syndrome
Polycystic disease of kidney and liver presenting in childhood.
X-linked spondyloepiphyseal dysplasia tarda: clinical and linkage data.
A prisoner with an unusual karyotype (46,XY,Dq-).
An extra small metacentric chromosome in association with multiple congenital abnormalities.
Genetic Concepts and Neoplasia
Elements of Medical Genetics
Congenital hypothyroidism and hyperthyroidism in monozygotic twin girls.
A patient with 45,X-46,XXq--46,XXq-dic karyotype.
A partial D-trisomy-normal mosaic female.
A case of 48,XXY,21+ in an infant with Down's syndrome.
An inherited 1;G translocation.
The 'law of ancestral heredity' and the Mendelian-ancestrian controversy in England, 1889-1906.
Correspondence
Genetic-epidemiological studies in progressive muscular dystrophy.
Chromosome studies in selected spontaneous abortions. Polyploidy in man.
Fertility in balanced heterozygotes for a familial centric fusion translocation, t(DgDg).
A complex chromosomal rearrangement with formation of a ring 4.
Additional G-like chromosome in a malformed boy.
Alzheimer's Disease and Related Conditions
Haemoglobin Osu-Christiansborg: a new beta-chain variant of haemoglobin A ( beta52 (D3) aspartic acid leads to asparagine) in combination with haemoglobin S.
The 13q- deletion syndrome.
Somatic stigmata of Turner's syndrome in a patient with 46,XXq-.
A case of cri-du-chat associated with cataracts and transmitted from a mother with a 4-5 translocation.
Trisomy 18 in one of fraternal twins.
Human Genetics and Medicine
Xg groups and sex abnormalities in people of northern European ancestry. northern European ancestry
On the distribution of phenotypes in XXY males and their parents.
ABH secretor status of the fetus: a genetic marker identifiable by amniocentesis.
A ring-4 chromosome in a patient with normal intelligence and short stature.
Additional evidence of gradual loss of germ cells in the pathogenesis of streak ovaries in Turner's syndrome.
The Distribution of the Blood Groups in the United Kingdom
Serendipity in St. Helena. A Genetical and Medical Study of an Isolated Community
Corrigendum
Klinefelter's syndrome and G trisomy.
Remarkable Facts in Human Albinism and Leukism