Journal of Medical Genetics - 1978

134 articles | Last updated: 2025-12-03 14:12:57
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T A T A T A T A
Haemoglobin H disease in 2 Filipino families.
Chromosome banding studies in two patients with XXXXY syndrome.
Translocation of chromosome 4 and 9 with ring formation of chromosome 4 short arm.
Computerised chromosome data bank
Developmental Biology and Pathology. (Current Topics in Pathology.)
The Gardner syndrome: a cell culture study on kindred 109.
On the relation between malaria and G-6-PD deficiency: a reply
Down syndrome and recent demographic trends in Manitoba.
Clinical experience with trisomies 18 and 13.
Atlas des Maladies Chromosomiques
Linkage relations of a locus for congenital total nuclear cataract.
First premarital screening of thalassaemia carriers in intermediate schools in Latium.
Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism
Population heterogeneity in human sperm DNA content.
Epiphysial dysplasia: a constant finding in the XXXXY syndrome.
Heterozygote advantage for the phenylketonuria allele.
Oral Facial Genetics
The Eye in Chromosome Duplications and Deficiencies
Molecular Anthropology. Genes and Proteins in the Evolutionary Ascent of the Primates
Medical Genetics. Proceedings of the Symposium at Debrecen-Hajduszoboszlo, Hungary, 27-29 April, 1976
Pericentric inversions inv(2)(p11q13) and inv(2)(p13q11) in 2 unrelated families.
47,XX,+der(18),t(9;18)(p24;q21) mat: a distinct partial trisomy 18q--syndrome?
The phenotype Ae1B: a probable result of chimerism.
Absent left hemidiaphragm, arhinencephaly, and cardiac malformations.
Thalassaemia of intermediate severity resulting from the interaction between alpha- and beta-thalassaemia.
Partial trisomy 6p with karyotype 46,XY,der(22), t(6;22)(p22;q13)mat.
Comment.
Validation and aplication of an interval factor in estimating age at onset of Huntington's disease.
Use of overlapping normal distributions in genetic counselling.
Genetic counseling of consanguineous families. Use of Smith's method to calculate recurrence risks in multifactorial inheritance in consanguineous matings.
Partial trisomy 18 in a family with a translocation (18;21)(q21;q22).
Familial radioulnar synostosis.
Cellular content of amniotic fluid as predictor of central nervous system malformations.
Brachydactyly, distal symphalangism, scoliosis, tall stature, and club feet: a new syndrome.
Acute myelogenous leukaemia in Hurler's syndrome.
Genetic study of narcoleptic syndrome.
Question and answer
Guidelines for Research Involving Recombinant DNA Molecules
Immunology for the Practising Physician
On the relation between malaria and G-6-PD deficiency
Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16.
Apical systolic click and murmur associated with neurofibromatosis.
Placentation, anencephaly, and spina bifida.
Biochemical Methods in Medical Genetics
Errata
Thalassaemia types and their incidence in Sardinia.
Taurodontism and Klinefelter's syndrome.
X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies.
Prenatal diagnosis of a de novo Y/22 translocation.
The Aase syndrome in a female infant.
Supernumerary small ring chromosome.
Genetic family history questionnaire
E1k, another quantitative variant at cholinesterase locus 1.
Raised alpha-fetoprotein levels in amniotic fluid and maternal serum associated with distension of the fetal bladder caused by absence of urethra.
Primary hypogonadism in the Borjeson-Forssman-Lehmann syndrome.
Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation.
Medico-Social Management of Inherited Metabolic Disease
Shifting genetic patterns in anencephaly and spina bifida.
Unusual inheritance of Becker type muscular dystrophy.
Recessively inherited costovertebral segmentation defect with mesomelia and peculiar facies (Covesdem syndrome): A new genetic entity?
Fertility in 47,XXX and 45,X patients.
Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromes.
Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicism.
A family study of vesicoureteric reflux
Parthenogenesis.
Hereditary pancreatitis in England and Wales.
Nephrogenic diabetes insipidus and Werdnig-Hoffmann disease in a child: an unusual association.
Late discovery of a case of testicular feminisation.
Calculation of genetic risks in Duchenne muscular dystrophy by geneticists in the United Kingdom.
Combined use of alphafetoprotein and amniotic fluid cell morphology in early prenatal diagnosis of fetal abnormalities.
Length heteromorphisms of fluorescent (f) and non-fluorescent (nf) segments of human Y chromosome: classification, frequencies, and incidence in normal Caucasians.
Bilateral renal agenesis in 2 male sibs born to consanguineous parents.
Neural tube defects in New South Wales, Australia
Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy.
Familial atypical multiple mole-melanoma syndrome.
Segregation of an insertional chromosome rearrangement in 3 generations.
Trisomy 21 with 47,+18 lymphocyte cell line: double mitotic nondisjunction.
Triplication of a short arm region of chromosome 15.
Reproduction in a woman with mosaicism.
Osteosarcoma in a patient with Hutchinson-Gilford progeria.
Predisposition to spina bifida.
Risk of coeliac disease in children of patients and effect of HLA genotype.
Waardenburg-like features with cataracts, small head size, joint abnormalities, hypogonadism, and osteosarcoma.
Trisomy 8 syndrome.
Down's Anomaly 2nd ed
Chemical Mutagens. Principles and Methods for their Detection Vol. 4
Advances in Human Genetics. Vol. 7
Hereditary brachydactyly with nail dysplasia.
De novo simultaneous reciprocal translocation and deletion.
Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome.
Autosomal recessive postaxial polydactyly type A in a Sicilian family.
Linkage studies in Van der Woude syndrome.
Necropsy of original case of Lowry's syndrome.
Inconsistent expression of both centromeres of a dicentric Y chromosome in a child with ambiguous external genitalia.
Linkage analysis in dominant acrocephalosyndactyly.
Myotonia Congenita and Syndromes Associated with Myotonia. Clinical-Genetic Studies of the Nondystrophic Myotonias
Introduction to Biometrical Genetics
Clinics in Rheumatic Diseases, Vol. 3, No. 2. Immunogenetics and Rheumatic Disease
Le Polymorphisme Biochimique et Les Facteurs de Son Maintien
Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy.
Genetics of adolescent idiopathic scoliosis.
A report on genetic registers. Based on the report of the Clinical Genetics Society Working Party.
Report of a mucopolysaccharidosis occurring in Australian aborigines.
Simplified classification of spontaneous abortions.
The Axenfeld syndrome and the Rieger syndrome.
Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome.
Principles of Genetic Counselling
Population Cytogenetics: Studies in Humans
A new type of chondrodystrophic mutant in the mouse.
Significance of detection of extra metacentric microchromosome in amniotic cell culture.
Cleft palate and accessory metacarpal of index finger syndrome: possible familial occurrence.
Inducibility of aryl hydrocarbon hydroxylase in cultured human lymphocytes: a study of repeatability.
Deletion 14q and pericentric inversion 14.
Meckel's syndrome (dysencephalia splanchno-cystica) in two Pakistani sibs.
Training of medical geneticists.
Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family.
Family studies of relation between Perthes disease and congenital dislocation of the hip
Complete trisomy 5p
Dominance in human genetics.
Oral Manifestations of Inherited Disorders
Gene-Environment Interaction in Common Diseases. Proceedings of the Symposium on Gene-Environment Interaction in Common Diseases held February 11-12, 1976, Tokyo
Spontaneous regression of metastatic malignant melanoma in 2 sibs with xeroderma pigmentosum.
A new form of Niemann-Pick disease characterised by temperature-labile sphingomyelinase.
Genetic studies of acute infantile spinal muscular atrophy (SMA type I). An analysis of sex ratios, segregation ratios, and sex influence.
Segregation analysis of chronic childhood spinal muscular atrophy.
Angiokeratoma corporis diffusum (Anderson-Fabry disease) in a single large family in Nova Scotia.
Meckel syndrome and the prenatal diagnosis of neural tube defects.
A 'new' syndrome of mental retardation with characteristic facies and brachyphalangy.
Popliteal pterygium syndrome: a phenotypic and genetic analysis.
Experimental Biology and Medicine Cytogenetic aspects of Malignant Transformation
Dermatoglyphics in Medical Disorders
Heterozygote advantage for the phenylketonuria allele.
Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q).
The Marden-Walker syndrome.