Journal of Medical Genetics - 1968

105 articles | Last updated: 2025-12-03 14:12:57
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T A T A T A T A
ABO blood groups and leprosy.
Research on Genetics in Psychiatry
Antibodies to Biologically Active Molecules. Proceedings of the 2nd Meeting of the Federation of European Biochemical Societies
Human Population Cytogenetics
Norrie's Disease. A Congenital Progressive Oculo-acoustico-cerebral Degeneration
Introduction to Animal Physiology and Physiological Genetics
The Biology of Human Adaptability
Abnormality on paternal and maternal sides: observations in schizophrenia and manic-depression.
A structurally abnormal chromosome (46,XX,?17p+) associated with mental deficiency and congenital malformations.
Congenital microcephaly with hiatus hernia and nephrotic syndrome in two sibs.
Books and Monographs: A Neuropsychiatric and Genetical Investigation of Acute Intermittent Porphyria
Surveys, Symposia, and Transactions: Phenotypic Expression. Immunological, Biochemical, and Morphological
Arrhinencephaly associated with a deficiency involving chromosome 18.
Mongolism. Ciba Foundation Study Group No. 25
Progress in Biophysics and Molecular Biology, Vol. 16
Sex Chromosomes
The Chromosome. Structural and Functional Aspects
An Introduction to Medical Genetics
Haemoglobin Korle-Bu (beta 73 aspartic acid replaced by asparagine) showing one of the two amino acid substitutions of haemoglobin C Harlem.
Cytogenetic studies in a family with Waldenstrom's macroglobulinaemia.
Changing incidence of positive direct Coombs test in inbred NZB-BL mice.
A survey of sex chromatin abnormalities in mental hospitals.
Inheritance in epidermolysis bullosa letalis.
Genetic study of sample of 70 patients with myasthenia gravis.
Incidence of fibrocystic disease in Wessex.
Diverse chromosomal anomalies in a family.
Surveys, Symposia, and Transactions: Cell Differentiation
Ancell-Spiegler cylindromas (turban tumours) and Brooke-Fordyce Trichoepitheliomas: evidence for a single genetic entity.
Impaired pronation-supination of the forearm: an inherited condition.
Hereditary cup-shaped ears and the Pierre Robin syndrome.
The UFAW Handbook on the Care and Management of Laboratory Animals
An Atlas of Mammalian Chromsomes, Vol. 1
Human Chromosomes. An Illustrated Introduction to Human Cytogenetics
Hyperlipidaemic xanthomatosis. II. Mode of inheritance in 55 families with essential hyperlipidaemia and xanthomatosis.
Finger and palm prints in chromatin-positive males.
Karyotypes of cultured cells from foetal membranes of normal newborns.
A Comparative Osteological Study of the Ainu and the Australian Aborigines
An Epidemiological Survey of Skin Diseases, Tattooing, and Rheumatic Diseases as Exemplified Initially by the Prevalence of Psoriasis and Tattooing
Translocation in Human Chromosomes with Special Reference to Mental Retardation and Congenital Malformations
Multiple sclerosis: discordance in three pairs of dizygotic twins.
Amino acid patterns in cystinuric families.
Combination of hereditary elliptocytosis and heterozygous beta-thalassaemia: a family study.
Secretor status in asthma and hay fever.
An extra small metacentric chromosome in a mentally retarded boy.
Books and Monographs: Recent Results in Cancer Research
Surveys, Symposia, and Transactions: Symposium on Autoimmunity and Genetics
New Editions: The Causes of Evolution
Constancy of alpha-1-acid glycoprotein variants of Caucasian patients under conditions of severe stress.
Sex chromatin survey in mentally handicapped children in Mexico.
The Thread of Life
Further factors influencing Rh-immunization: II.
Mental retardation in a child with a long B-group chromosome.
The Genetic Code. The Molecular Basis for Genetic Expression
A family study of major central nervous system malformations in South Wales.
Genetic characteristics of families of XO and XXY patients, including evidence of source of X chromosomes in 7 aneuploid patients.
A family with D-D translocation.
Down's syndrome with an unusual karyotype.
Biochemical Genetics
Hereditary non-spherocytic haemolytic anaemia with post-splenectomy inclusion bodies and pigmenturia caused by an unstable haemoglobin Santa Ana-beta-88 (F4) leucine--proline.
Incidence of ABO and RH blood groups in pulmonary tuberculosis in different ethnic groups.
ABO blood groups and vitiligo.
Further observations on Kell blood groups in families ascertained via a mongol propositus.
A large deletion of chromosome no. 1 (46,XY,1?--).
Books and Monographs: Clinical Genetics in Psychiatry. Problems in Nosological Classification
Books and Monographs: Humangenetik. Ein kurzes Handbuch in funf Banden. Band I/1 Grundlinien, Terminologie, Methoden, Geschichte der Humangenetik, Abstammungsgeschichte, Chromosomen, Mass und Formmerk
Surveys, Symposia, and Transactions: Social and Genetic Influences on Life and Death
An unusual karyotype in a patient with signs suggestive of Down's syndrome.
Medical Cytogenetics
Inherited diseases of the inner ear in man in the light of studies on the mouse.
Genetical studies in testicular feminization syndrome.
New translocation in three generations of a family.
XYY sex chromosomes in a Jamaican with orthopaedic abnormalities.
The Clinical Pathology of Infancy
Karyotyp and Phanotyp der autosomalen Chromosomenarberrationen beim Menschen
Anhidrotic ectodermal dysplasia: autosomal dominant inheritance with palate and lip anomalies.
X-linked hydrocephalus.
Multiple anomalies associated with a small extra metacentric autosome.
Books and Monographs: The Origin of Life
Surveys, Symposia, and Transactions: Annual Review of Genetics, Volume 1, 1967
Dermatoglyphs in human polyploidy.
Satellite association and trisomy in thyrotoxicosis.
Lost chromosomes in endometrial cells.
Aspects of Medical Virology
Human Radiation Cytogenetics
Protein Biosynthesis and Problems of Heredity, Development, and Ageing
Modern Genetics
Familial Interrelatedness in a Swedish Rural Population
The Placenta in Twin Pregnancy
Testosterone excretion rates in normal males and males with an XYY complement.
Familial microtia with meatal atresia in two sibships.
Books and Monographs: Biological Psychiatry
Books and Monographs: Sex Chromosomes and Sex Linked Genes
Surveys, Symposia, and Transactions: Proceedings of the Third International Congress of Human Genetics
Surveys, Symposia, and Transactions: Primates in Medicine
Surveys, Symposia, and Transactions: Pathogenesis of Nervous and Mental Diseases in Children
Surveys, Symposia, and Transactions: Probleme der molekularen und allgemeinen Biologie der Zelle. 3.Gesamttagung der Deutschen Gesellschaft fur experimentelle Medizin
Hyperlipidaemic xanthomatosis. I. Increased risk of death from ischaemic heart disease in first degree relatives of 53 patients with essential hyperlipidaemia and xanthomatosis.
Die Evolution der Organismen. Band I. Ergebnisse und Probleme der Abstammungslehre 3rd ed
Xg blood groups of 78 patients with Klinefelter's syndrome and of some of their parents.
Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome.
Diagnostic and genetical aspects of tuberous sclerosis.
Males with an XYY sex chromosome complement.
Surveys, Symposia, and Transactions: Progress in Medical Genetics
Surveys, Symposia, and Transactions: Comptes Rendus du 1er Congres International de Neurogenetique et Neuro-optalmologie
New Editions: Genetics for Medical Students