| Karyotype-phenotype Correlations in Gonadal Dysgenesis and Their Bearing on the Pathogenesis of Malformations |
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| Copper Content of Hair in Normal Families and those with Wilson's Disease |
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| Patterns of Initiation of DNA Replication in Cultured Cells from Human Females |
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| Intestinal Polyposis. (Galton Laboratory Memoirs No. 40.) |
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| Genetics of human blood coagulation. |
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| Blood and Serum Groups in Taiwan |
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| Culture of Peripheral Blood Leucocytes for Chromosome Analysis using a Few Drops of Whole Blood |
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| Human Haemoglobins |
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| Genetics Today. Proceedings of the XI International Congress of Genetics, The Hague, The Netherlands, September 1963. Volume 2: Reports, Records and Plenary Sessions. Symposia 1-13. Volume 3: Symposia |
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| Congenital Hereditary Lymphoedema |
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| Epidermolysis bullosa. |
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| Corrigendum |
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| Chromosome mosaicism in a hermaphrodite. |
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| Book Reviews |
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| ABO Blood Groups and Gastric Ulcer |
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| Cerebro-metacarpo-metatarsal Dystrophy (Pseudo-Pseudo Hypoparathyroidism) with Chromosomal Anomaly |
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| Muscular Dystrophy (Duchenne) in a Girl with Turner's Syndrome |
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| Segregation Analysis of Juvenile Diabetes Mellitus |
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| Down's Syndrome. A Clinical and Cytogenetical Investigation |
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| Corrigenda |
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| Resistance of A/Jax Mouse Embryos with Spontaneous Congenital Cleft Lip to the Lethal Effect of 6-Aminonicotinamide |
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| Familial Occurrence of Myxoedema |
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| Symposium on Advanced Medicine. Proceedings of a Conference held at the Royal College of Physicians of London November 16-20, 1964 |
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| Le Message Hereditaire |
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| Familial Low Birthweight Dwarfism with an Unusual Facies and a Skin Eruption |
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| The Relative Length and Arm Ratio of the Human Late-replicating X Chromosome |
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| Leucocyte Alkaline Phosphatase in Klinefelter's Syndrome |
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| Chromosome Mosaicism in an Indian Child with Down's Syndrome |
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| Foam-cell Reticulosis of Mice: An Inherited Condition Resembling Gaucher's and Niemann-Pick Diseases |
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| Duchenne's Muscular Dystrophy and the Xg Blood Groups: a Search for Linkage |
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| Association of Leukaemia and Blood Groups |
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| Family studies and aetiology of club foot. |
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| A masculinizing syndrome associated with a doubly-satellited extra chromosome. |
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| Assessment of two macromethods and three micromethods of culturing human white blood cells for chromosome analysis. |
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| Muscle Histology in Carriers of Duchenne Muscular Dystrophy |
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| The Chemical Origin of Life |
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| A Genetic Study of Stub Thumbs among Various Ethnic Groups in Israel |
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| A Probable Case of Incomplete Trisomy of a Chromosome of the 13-15 Group |
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| Humangenetik. Ein Kurzes Handbuch in funf Banden. Vol. 3, No. 1 |
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| Blood Groups and Urinary Micro-organisms |
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| Familial Occurrence of Trisomy 16-18 |
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| Ovarian Dysgenesis and Presumed Isochromosome of the Long Arm of X |
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| Elements of The Natural Movement of Population |
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| Genetic factors in diabetes mellitus studied by the oral glucose tolerance test. |
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| Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency, Thalassaemia, and Abnormal Haemoglobins in Taiwan |
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| Monozygotic Twinning in Mice |
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| Introduction to Medical Genetics |
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| Smallpox Vaccination: ABO and Rhesus Blood Groups |
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| Confirmation of Association Between ABO Blood Groups and Salivary ABH Secretor Phenotypes and Electrophoretic Patterns of Serum Alkaline Phosphatase |
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| Incidence and Family Aggregation of Major Congenital Malformations of Central Nervous System |
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| Changes in the Chromosome and Haemoglobin Patterns in a Patient with Erythro-leukaemia |
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| Human Diversity. The nature and significance of differences among men |
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