| Proceedings of a Symposium on Scoliosis |
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| Principles of Medical Statistics |
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| Ring chromosome 18 in a patient with multiple anomalies. |
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| Chromosome mosaicism in a mentally retarded mother and her daughter. |
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| Genetics of Interracial Crosses in Hawaii |
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| The Chromosomes of the Algae |
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| Corrigenda |
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| Congenital Malformations |
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| The Genetics of Neurological Disorders |
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| Immunological Aspects of Viral Oncolysis |
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| Chicago Conference 1966: Standardization in Human Cytogenetics |
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| Vascular disease of the central nervous system in Wales. |
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| Endocrine Genetics |
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| Xg blood group frequencies in some further populations. |
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| Programed Genetics |
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| Combination of spherocytosis and a variant of beta thalassaemia ('isolated raised Hb A2'). |
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| Ovarian dysgerminoma in three generations? |
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| Die Chromosomenstruktur des Menschen in Mitosis und Meiosis |
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| Serum alkaline phosphatase types in North American indians and negroes. |
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✓ |
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North American indians and negroes |
| Humangenetick: Ein kurzes Handbuch in funf Banden |
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| Skeletal hand charts in inherited connective tissue disease. |
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| Genetics of ankylosing spondylitis. |
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| Latent cystathioninuria. |
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| Influence of the Y chromosome on gonadal differentiation: asymmetrical gonads in an XO-XY mosaic. |
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| Presumptive Y/D translocation in mixed gonadal dysgenesis. |
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| The Living Races of Man |
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| Blood groups and leprosy. |
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| Leprosy and ABO blood groups. |
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| Congenital Hereditary Lymphoedema in the Dog. Part I--Clinical and Genetic Studies |
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| De Lange Syndrome: Report of a Case with an Unusual Karyotype |
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| The Sex Chromatin |
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| A sex chromatin survey of newborn children in two London hospitals. |
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| An infant with multiple congenital anomalies and a ring chromosome in group C (X-6-12). |
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| A myotonic syndrome associated with Klinefelter's syndrome. |
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| Haemoglobin J Tongariki (alpha-115 alanine--aspartic acid): the first new haemoglobin variant found in a Pacific (Melanesian) population. |
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| Agar diffusion test for serum cholinesterase typing and influence of temperature on dibucaine and fluoride numbers. |
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| Age, sex, and ABO blood group distributions of 150 patients with cerebral arteriovenous aneurysms. |
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| A familial variant chromosome in the 13-15 group. |
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| Advances in Blood Gouping II |
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| Les Chromosomes Humains (caryotype normal et variations pathologiques) |
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| Heritage from Mendel |
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| Hypoplastic left heart complex. |
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| High incidence of haemoglobin G Accra in a rural district in Jamaica. |
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| Chromosomes of human endometrium. |
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| Factors Influencing the Immunization of Rh-negative Mothers |
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| Biochemical Genetics |
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| Pseudocholinesterasen Pharmakgenetik; Biochemie; Klinik |
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| Mendelian Inheritance in Man. Catalogs of Autosomal Dominant, Autosomal Recessive, and X-linked Phenotypes |
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| Concordance and discordance of congenital heart disease in 20 families. |
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| Leucocyte alkaline phosphatase and erythrocyte glucose-6-phosphate dehydrogenase in Down's Syndrome. |
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| Diabetes in wales. |
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| Hematologie Geographique. Ecologie Humaine Caracteres Hereditaires du Sang |
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| Endemic goitre in Greece: a study of 379 twin pairs. |
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| Myotonic dystrophy and polycystic disease of the kidneys. |
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| Human polymorphism. |
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| Finger Prints |
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| Monographs in Human Genetics, 2 |
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| Abhandlungen uber die Pathophysiologie der Regulationen |
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| The Chromosome Disorders. An Introduction for Clinicians |
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| Sex Determination |
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| Handbuch der Haut-und Geschlechtskrankheiten |
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| The Role of Chromosomes in Development |
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| A new translocation between chromosomes in the 6-12 and 21-22 groups. |
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| A Case of Translocation (C/14) with Mental Retardation in Two Offspring |
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| Human Genetics |
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| Coronary artery disease in Wales. |
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| Anomalies of development in a girl with unusual sex chromosomal mosaicism. |
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| Transferrin variants in Greeks. |
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| Comparison of mitotic growth rates of human capillary whole blood cultured in a variety of media. |
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| Man's Haemoglobins Including the Haemoglobinopathies and their Investigation |
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| Humangenetik. Ein kurzes Handbuch in funf Banden |
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| Genetics of the Dombrock blood group system. |
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| A patient with 45XO-48XYYY mosaicism. |
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| The Genetics of Gastro-intestinal Disorders |
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| Current Studies in Hemophilia |
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| Malignant Transformation by Viruses |
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| Variation in Chemical Composition of the Nervous System as Determined by Developmental and Genetic Factors |
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| Congenital Hereditary Lymphoedema in the Dog Part II--Pathological Studies |
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| General Cytology |
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| Idiopathic scoliosis: genetic and environmental aspects. |
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| Epidermolysis bullosa dystrophica, hypoplastic type, associated with Pelger-Huet anomaly. |
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| Morphogenese Pathologique. Des Monstruosites aux Malformations |
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| Experimental red cell chimerism in the heterozygote (Wvw) of the W-series mutants in the house mouse. |
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| Trisomy D1 (13-15) associated with XO-XY mosaicism. |
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| Progress in Medical Genetics, Vol. IV |
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| Hydronephrosis in mouse, rat, and man. |
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| Determinants of Sex Proportions in Man, with Consideration of the Evidence Concerning a Contribution from X-linked Mutations to Intrauterine Death |
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| A second heterozygote for 'silent' and 'fluoride resistant' genes for serum cholinesterase. |
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| Chromosome Studies on Adults |
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