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