Journal of Medical Genetics - 1972

129 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
Conenital hypothyroidism in association with a ring chromosome 18.
Chemical Mutagenesis in Mammals and Man
Lionel Sharples Penrose (1898-1972), MA,MD,DSc,FRCP,FRS.
46,Xinv(Yp+q-) in four generations of an Indian family.
Unstable haemoglobin Koln disease in members of a Malay family. Malay
Genetical, Functional, and Physical Studies of Hemoglobins
Trisomy G/Normal Mosaicism. A Cytological and Clinical Investigation
Reciprocal chromosome translocations: analysis of two mutants by interactive computer.
The nature and inheritance of Kirner's deformity.
The effect of absence of thumb on palmar dermatoglyphics.
The Role of Genetics in Mental Retardation
Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques.
The Genetics of Mental Disorders
Papers on Regulation of Gene Activity During Development
The incidence and genetics of cystic fibrosis.
The value of investigations of the incidence of peptic ulcer in the families of patients with duodenal ulcer.
Development of humoral and cellular immunity in man.
Mongolism and sex: a common problem of cell proliferation? Mongolism
A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome.
Blood enzymes in the de Lange syndrome.
Congenital absence of the fibula and craniosynostosis in sibs.
Ecological Genetics and Evolution
Giemsa banding pattern of a heritable 1q+ variant chromosome: a possible partial duplication.
Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).
Immunoglobulin abnormality in a girl with a large chromosome 18.
A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother.
A rare blood group antigen An a (Ahonen).
Erythrocyte acid phosphatase polymorphism and haemolysis.
Familial cancer of the colon and rectum.
Comparative Genetics in Monkeys, Apes and Man
Inherited pericentric inversion of a group D (13-15) chromosome.
A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype.
True hermaphroiditism: cytogenetic analysis, surgical repair, and social implications.
Two cases of trisomy D associated with adrenal tumours.
Nystagmus in a female carrier of ocular albinism.
Birth Defects: Original Article Series, VII, 1
Genetical investigations in dyslexia.
Antinuclear factor in rapid and slow acetylator patients treated with isoniazid.
The use of the autoanalyzer to determine the acetylator phenotype.
A syndrome of mental and physical etardation, speech disorders, and peculiar facies in two sisters.
Camurati-Engelmann disease. Genetics and clinical manifestations with a review of the literature.
A family study of Fallot's tetralogy.
Camptodactyly: occurrence in two new genetic syndromes and its relationship to other syndromes.
Recessively inherited myotonia congenita.
A case of double aneuploidy, 47,XXY,14-,t(13q14q)+, also probably homozygous for the cystic fibrosis gene.
Immunological studies in congenital nephrosis.
Corrigenda
Antenatal development of amylase isoenzymes.
The inheritance of dental traits in a Chinese population in the United Kingdom.
A Psychological-Psychiatric Study of Patients with Klinefelter's Syndrome, 47,XXY
Diagnosis of Metabolic Eye Diseases
A new genetic variant of the spinal muscular atrophies in infancy.
Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families.
Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.
Congenital leukaemia with 46,XX,t(Bq+,Cq-) cells.
Turner's syndrome with menstruation.
A Duarte variant with clinical signs.
A twin study of the genetic influences on the electroencephalogram.
Autosomal dominant inheritance and amino aciduria in Blackfan-Diamond anaemia.
The autosomal recessive variety of congenital stationary night-blindness with myopia.
Twin heritability study of the effect of corticosteroids on intraocular pressure.
ABO incompatibility as a cause of spontaneous abortion: evidence from abortuses.
Rural-urban differentials in consanguinity.
Incidence and genetics of Legg-Perthes disease (osteochondritis deformans) in British Columbia: evidence of polygenic determination.
Triple X female and a Down's syndrome offspring.
Double aneuploidy (47,XX,21+-45,X) arising through simultaneous double non-disjunction.
Corrigenda
Gene duplication, mutation load, and mammalian genetic regulatory systems.
The use of new staining techniques for human chromosome identification.
Cytogenetic survey of XYY males in two juvenile court populations, with a case report.
Genetic heterogeneity for dystrophia myotonica.
Dominant ectrodactyly and possible germinal mosaicism.
X-linked mental retardation without physical abnormality (Renpenning's syndrome) in sibs in an institution.
Superior intelligence in sighted retinoblastoma patients and their families.
Genetic aspects of selective immunoglobulin A deficiency.
Normal male development with Y chromosome long arm deletion (Yq-).
A ring-20 chromosome.
The Genetics of Human Populations
Bibliographica genetica medica
Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals.
Palmar dermatoglyphs in tuberous sclerosis.
Bone marrow chromosomes in Fanconi's anaemia.
Down's syndrome with an atypical G-G translocation derived from familial pericentric inversion in one chromosome of the G group.
Biomathematics
Molecular Genetics. An Introductory Narrative
Probability Models and Statistical Models in Genetics
Pyloric atresia. A hereditary congenital anomaly with autosomal recessive transmission.
Haemoglobin Ocho Rios ( beta52 (D3) aspartic acid leads to alanine): a new beta-chain variant of haemoglobin A found in combination with haemoglobin S.
A new G-6-PD variant associated with chronic non-spherocytic haemolytic anaemia in a negro family. negro
The polymorphic acetylation of sulphapyridine in man.
Syndrome of pigmentary retinal degeneration, cataract, microcephaly, and severe mental retardation.
A case of 48,XXXX female with normal intelligence.
Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism.
Multiple congenital defects associated with an abnormal unclassifiable karyotype.
Cri-du-chat syndrome combined with partial C-group trisomy.
A sex chromatin study of Chinese school children.
Familial chronic muco-cutaneous candidiasis.
48,XYYY: a new syndrome?
A double aneuploid mosaic: trisomy 13 and XXY.
Immunogenetics
Pedigrees with diabetes insipidus, diabetes mellitus, and optic atrophy.
Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease.
Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells.
A new HGPRT-deficient phenotype?
Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adult.
Coefficients of Natural Selection
Cytoenzymology and Isozymes of Cultured Cells
Hereditary Sensory Radicular Neuropathy
Genes, Dreams and Realities
A statistical study of half-sibships born to parents affected with Huntington's disease.
Familial correlations for age at onset and age at death in Huntington's disease.
Variation in secretor and Lewis type frequencies within the British Isles.
ABH secretor and Lewis type frequencies in an Icelandic series.
Abnormalities of the electrocardiogram in hereditary myopathies.
Serum iron and unsaturated iron-binding capacity in the -thalassaemia trait: their relation to the levels of haemoglobins A, A 2 , and F.
Searching for XYY males through electrocardiograms.
A human ring C chromosome associated with multiple congenital abnormalities.
Messenger RNA in animal cells.
Early Diagnosis of Human Genetic Defects--Scientific and Ethical Considerations
The Dombrock system: linkage relations with other blood group loci.
Christmas disease in one of a pair of monozygotic twin girls, possibly the effect of lyonization.
Apparent G-monosomy, G-deletion, and incomplete Down's syndrome in a single family.
Progress in Medical Genetics, Vol. 8
The dominant and recessive forms of cutis laxa.
Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form.
Correspondence
The Bacteriophage Lambda
Addendum
Aminoacidopathies, Immunoglobinopathies, Neuro-genetics and Neuro-ophthalmology