| Glucose-6-phosphate dehydrogenase (G6PD) deficiency, abnormal haemoglobins, and thalassaemia in Yugoslavia. |
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| Genetic Polymorphism. (All Souls Studies V.) |
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| Satellite association and translocation mongolism. |
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| Book Reviews |
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| Book Reviews |
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| ABO blood groups and cirrhosis of the liver. |
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| Bimodal distribution of erythrocytes in heterozygotes for strong Mediterranean glucose-6-phosphate dehydrogenase deficiency. |
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| Hereditary contractures of the fingers (camptodactyly). |
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| Haemoglobin genotypes, ABO blood groups, and Burkitt's tumour. |
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| Homocystinuria: an observation on the inheritance of cystathionine synthase deficiency. |
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| The use of the surname as a genetic marker in Wales. |
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| A monopodal sireniform monster with dermatoglyphic and cytogenetic studies. |
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| Distribution of Haptoglobin Subtypes in Greeks |
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Greeks |
| Monozygotic twins of different sex. |
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| 13-15 trisomy mosiacism in a normal-looking 14-year-old retarded girl. |
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| Hypertrichosis terminalis with simian characteristics. |
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| Chromosome studies in familial leukaemia. |
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| Blood group changes in leukaemia. |
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| The Increased Risk of Death from Ischaemic Heart Disease in First Degree Relatives of 121 Men and 96 Women with Ischaemic Heart Disease |
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| Family Studies on Ocular Refraction and Its Components |
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| Astrocytomas and the ABO Blood Groups |
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| Huntington's Chorea |
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| Malformations Associees de la Tete et des Extremites |
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| Pyridoxine-responsive anaemia determined by an X-linked gene. |
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| The 45XO/46XY mosaic intersex syndrome. |
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| Turner's syndrome: further demonstration of the presence of specific cognitional deficiencies. |
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| Chromosome mosaicism in a child with features characteristic of the 'Cat Cry' syndrome. |
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| Detection of chromosomal mosaicism by computer methods. |
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| Chromosome preparation from leucocyte culture. A simplified method for collecting samples by post. |
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| Book Reviews |
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| An XO-X ring X chromosome mosaicism in an individual with normal secondary sexual development. |
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| Oral-facial-digital syndrome, with polycystic kidneys and liver: pathological and cytogenetic studies. |
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| Genetics of the Norway Rat |
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| Teach Yourself Genetics |
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| Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy. |
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| Expectation of abnormality on paternal and maternal sides: a computational model. |
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| Turner's Syndrome in a Phenotypic Male with XO/XY Mosaicism and Autosomal Aberrations |
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| Apparent deletion of X chromosome in a prepuberal girl. |
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| Corrigendum |
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| Apparent Monosomy of a G Autosome in a Jamaican Infant |
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| An Extra Small Metacentric Chromosome in a Female Child |
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| The Metabolic Basis of Inherited Disease, 2nd ed |
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| Incidence of congenital pyloric stenosis in Malta. |
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| Diagnosis and Genetics of Defective Colour Vision |
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| Turner's syndrome in monozygotic twins. |
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| Klinefelter's syndrome with a presumptive deleted X chromosome. |
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| British Medical Bulletin |
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| The Early Conceptus, Normal and Abnormal. Papers and Discussions Presented at a Symposium held at Queen's College, Dundee, September 17th, 18th, and 19th, 1964 |
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| Vergleichende Untersuchungen uber die Haufigkeit angeborener menschlicher Missbildungen |
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| A proposed classification of genetically determined mosaicism in man. |
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| Quantitative Variations of Haptoglobins in a Caucasian Family |
✓ |
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| Symphalangism: A Pedigree from South India |
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| Sex-linked cleft palate. Report of a family and review of 77 kindreds. |
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| Juvenile polyposis coli. |
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| Gonadal dysgenesis and ulcerative colitis. A case report with clinical, cytogenetic, and post-mortem studies. |
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| Down's syndrome with a familial D/D reciprocal translocation and a G/G chromosome. |
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| Congenital anomalies due to transmission of a chromosome translocation. |
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| A family showing transmission of a translocation between a 6-12 chromosome and a 21-22 chromosome. |
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| ABO and rhesus blood group distribution among patients attending veneral diseases clinics. |
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| Twins in sibships with Klinefelter's syndrome. |
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| Bloch-Sulzberger Syndrome (incontinentia pigmenti). |
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| Epiloia (tuberous sclerosis): a report of a case with unusual tumours. |
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| Congenital asymmetry. |
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| A family study of the late infantile and juvenile forms of metachromatic leucodystrophy. |
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| The X-linked blood group system Xg tests on British, Northern American, and northern European unrelated people and families. |
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northern European; British; Northern American |
| Gene effect in carriers of anhidrotic ectodermal dysplasia. |
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| The silent gene for serum pseudocholinesterase. |
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| A pair of twins, one of whom has chronic granulocytic leukaemia. |
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| Renal Tubular Dysfunction |
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| A Complex Pattern of Chromosome Abnormalities in the Acute Phase of Chronic Granulocytic Leukaemia |
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| Haptoglobin Phenotypes Among Egyptians |
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| A Fatal Congenital Defect Associated with a Unique Chromosome Abnormality |
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| An unstable ring chromosome in a female infant with hypotonia, seizures, and retarded development. |
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| Genetic diversity in serum albumin. |
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| Familial Camptodactyly with Taurinuria |
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| New Directions in Human Genetics. A Symposium |
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| Die Angeborenen Fehlbildungen der Hand und ihre Operative Behandlung |
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