Journal of Medical Genetics - 1975

98 articles | Last updated: 2025-12-03 14:12:57
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T A T A T A T A
Personality Differences and Biological Variations. A Study of Twins
SI Units
The occurrence of gonadal dysgenesis in association with monozygotic twinning.
Amniotic fluid macrophages and the antenatal diagnosis of anencephaly and spina bifida.
Letter: Mutation as the source of the abnormal gene for plasma cholinesterase.
A genetic study of torsion dystonia.
Aglossia-adactylia syndrome.
Two family studies on congenital dislocation of the hip after early orthopaedic screening Hungary.
Alpha-feto-protein during development and in disease.
Nucleus and Cytoplasm, 3rd ed
Specific chromosome aberrations in ataxia telangiectasia.
Homozygous haemoglobin D Punjab.
A new case of haemoglobin Bucuresti in a Cuban family: further functional studies.
Klinefelter's syndrome associated with a D/D translocation.
Handbuch der Inneren Medizin, vol 7--Erbliche Defekte des Kohlenhydrat-Aminosauren-und Proteinstoff-wechsels
Polydactyly and brachymetapody in two English families.
Genetics of the complement system.
Trisomy 13 and Rubinstein-Taybi syndrome.
Clinical and ultrastructural observations in a kindred with normo-hyperkalaemic periodic paralysis.
Thalassaemia in northern Liberia. A survey in the Mount Nimba area.
A family with apparently sex-linked optic atrophy.
The mechanism of genetic predisposition in congenital dislocation of the hip.
Population studies on Gilbert's syndrome.
Cell membrane receptors for serological reagents.
Trisomy 22. Two new cases and delineation of the phenotype.
Birth Defects
The Genetics of Locomotor Disorders
Human Gene Mapping
Biomathematics, vol. 5--The Genetic Structure of Populations.
Attitudes of patients and their relatives to Huntington's disease.
Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells.
Congenital vertebral anomalies: aetiology and relationship to spina bifida cystica.
Ocular colobomata, cardiac defect, and other anomalies: a study of seven cases including two sibs.
Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat.
A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signs.
X-Linked Mental Retardation and Verbal Disability
Hirschsprung's disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly in sibs: a case for fetoscopy.
X-linked mental retardation associated with macro-orchidism.
Autosomal recessive oculopharyngeal muscular dystrophy.
Partial trisomy for the long arms of chromosome no. 5 due to insertion and further 'aneusomie de recombinaison'.
Bloom's syndrome: a probable new case with cytogenetic findings.
Oesophageal atresia in the South West of England.
A case of hyalinosis cutis et mucosae (lipoid proteinosis of Urbach and Wiethe) with common ancestors in four remote generations.
Distinction between Duchenne and other muscular dystrophies by ribosomal protein synthesis.
A family study of coeliac disease.
Haemoglobin Lepore Boston and elliptocytosis in a family of Indonesian-German ancestry. Indonesian-German ancestry
Deletion of the short arm of chromosome No. 10.
The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.
Homozygous beta thalassaemia in Liberia.
Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy.
A patient with congenital anomalies and a deletion of the long arm of the long arm of chromosome 4 [46,XY,del(4)(q31)].
A mentally retarded child with a translocation involving chromosomes 12 and 19.
Dicentric Y chromosome in mixed gonadal dysgenesis.
The XYY Syndrome and Klinefelter's Syndrome
Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-).
Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio.
Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature.
Differences in human X isochromosomes.
The Stickler syndrome presenting as a dominantly inherited cleft palate and blindness.
Skeletal Dysplasias
Neonatal testicular torsion in two brothers.
Letter: Klinefelter's syndrome and maternal XX/XXX mosaicism.
Letter: Hirschsprung's disease and congenital deafness.
Selected Screening Tests for Genetic Metabolic Diseases
Giemsa banding of chromosome 1gh+ and linkage analysis.
Estimation of the age at onset of Huntington's disease from factors associated with the affected parent.
Treatment of Parkinsonism--The Role of Dopa Decarboxulase Inhibitors.
Methods in Human Cytogenetics
Alpha1-antitrypsin phenotypes in sex chromosome mosaicism.
Identification of C trisomies in human abortuses.
Haemoglobin Hasharon in a north Italian community.
The Biology of Racial Integration
45,X Turner's syndrome in monozygotic twin sisters.
A family with an inherited translocation involving the no. 4/no. 21 chromosomes.
Stub thumbs
Trisomy 4q32 leads to 4qter due to a maternal 4/21 translocation.
Malformation Syndromes
Huntington's Chorea, 1872-1972
Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.
Carbohydrate metabolism in dystrophia myotonica.
Genetical components of physiological tremor.
Familial trisomy 7 mosaicism.
Transplacental passage of blood cells.
Development of dermal ridges in the fetus.
Haemoglobin Lepore in Cyprus.
A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-).
Practical Human Cytogenetics
Distal brachyphalangy of the thumb in mental retardation.
Trisomy of the short arm of chromosome 10.
HUMAN CYTOGENETIC REGISTRIES
Clinical Cytogenetics and Genetics
Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome.
Prenatal diagnosis of a neural tube defect: Meckel syndrome.
Einfuhrung in die Immonogenetik
Psychiatrie. Vol. 8. Die Erblichen Myoklonisch-Epileptische-Dementiellen Kernsyndrome.
Genetic factors in amyloidosis.
The search for relevant cell culture research in cystic fibrosis: one researcher's opinion.
Progress in Medical Genetics, Volume X