| Personality Differences and Biological Variations. A Study of Twins |
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| SI Units |
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| The occurrence of gonadal dysgenesis in association with monozygotic twinning. |
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| Amniotic fluid macrophages and the antenatal diagnosis of anencephaly and spina bifida. |
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| Letter: Mutation as the source of the abnormal gene for plasma cholinesterase. |
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| A genetic study of torsion dystonia. |
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| Aglossia-adactylia syndrome. |
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| Two family studies on congenital dislocation of the hip after early orthopaedic screening Hungary. |
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| Alpha-feto-protein during development and in disease. |
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| Nucleus and Cytoplasm, 3rd ed |
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| Specific chromosome aberrations in ataxia telangiectasia. |
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| Homozygous haemoglobin D Punjab. |
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| A new case of haemoglobin Bucuresti in a Cuban family: further functional studies. |
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| Klinefelter's syndrome associated with a D/D translocation. |
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| Handbuch der Inneren Medizin, vol 7--Erbliche Defekte des Kohlenhydrat-Aminosauren-und Proteinstoff-wechsels |
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| Polydactyly and brachymetapody in two English families. |
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| Genetics of the complement system. |
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| Trisomy 13 and Rubinstein-Taybi syndrome. |
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| Clinical and ultrastructural observations in a kindred with normo-hyperkalaemic periodic paralysis. |
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| Thalassaemia in northern Liberia. A survey in the Mount Nimba area. |
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| A family with apparently sex-linked optic atrophy. |
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| The mechanism of genetic predisposition in congenital dislocation of the hip. |
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| Population studies on Gilbert's syndrome. |
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| Cell membrane receptors for serological reagents. |
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| Trisomy 22. Two new cases and delineation of the phenotype. |
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| Birth Defects |
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| The Genetics of Locomotor Disorders |
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| Human Gene Mapping |
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| Biomathematics, vol. 5--The Genetic Structure of Populations. |
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| Attitudes of patients and their relatives to Huntington's disease. |
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| Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells. |
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| Congenital vertebral anomalies: aetiology and relationship to spina bifida cystica. |
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| Ocular colobomata, cardiac defect, and other anomalies: a study of seven cases including two sibs. |
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| Pseudohermaphroditism with clinical features of trisomy 19 in an infant trisomic for parts of chromosomes 16 and 18: 47,XY,der(18),t(16;18)(p12;q11)mat. |
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| A syndrome of hypohidrotic ectodermal dysplasia with normal teeth, peculiar facies, pigmentary disturbances, psychomotor and growth retardation, bilateral nuclear cataract, and other signs. |
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| X-Linked Mental Retardation and Verbal Disability |
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| Hirschsprung's disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly in sibs: a case for fetoscopy. |
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| X-linked mental retardation associated with macro-orchidism. |
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| Autosomal recessive oculopharyngeal muscular dystrophy. |
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| Partial trisomy for the long arms of chromosome no. 5 due to insertion and further 'aneusomie de recombinaison'. |
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| Bloom's syndrome: a probable new case with cytogenetic findings. |
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| Oesophageal atresia in the South West of England. |
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| A case of hyalinosis cutis et mucosae (lipoid proteinosis of Urbach and Wiethe) with common ancestors in four remote generations. |
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| Distinction between Duchenne and other muscular dystrophies by ribosomal protein synthesis. |
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| A family study of coeliac disease. |
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| Haemoglobin Lepore Boston and elliptocytosis in a family of Indonesian-German ancestry. |
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Indonesian-German ancestry |
| Deletion of the short arm of chromosome No. 10. |
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| The detection of carriers of benign (Becker-type) X-linked muscular dystrophy. |
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| Homozygous beta thalassaemia in Liberia. |
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| Dermatoglyphic findings in 54 triple-X females and a review of some general principles applying to the soles in sex chromosome aneuploidy. |
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| A patient with congenital anomalies and a deletion of the long arm of the long arm of chromosome 4 [46,XY,del(4)(q31)]. |
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| A mentally retarded child with a translocation involving chromosomes 12 and 19. |
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| Dicentric Y chromosome in mixed gonadal dysgenesis. |
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| The XYY Syndrome and Klinefelter's Syndrome |
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| Partial 9 trisomy by 3:1 segregation of balanced maternal translocation (7q+; 9q-). |
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| Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio. |
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| Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature. |
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| Differences in human X isochromosomes. |
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| The Stickler syndrome presenting as a dominantly inherited cleft palate and blindness. |
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| Skeletal Dysplasias |
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| Neonatal testicular torsion in two brothers. |
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| Letter: Klinefelter's syndrome and maternal XX/XXX mosaicism. |
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| Letter: Hirschsprung's disease and congenital deafness. |
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| Selected Screening Tests for Genetic Metabolic Diseases |
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| Giemsa banding of chromosome 1gh+ and linkage analysis. |
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| Estimation of the age at onset of Huntington's disease from factors associated with the affected parent. |
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| Treatment of Parkinsonism--The Role of Dopa Decarboxulase Inhibitors. |
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| Methods in Human Cytogenetics |
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| Alpha1-antitrypsin phenotypes in sex chromosome mosaicism. |
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| Identification of C trisomies in human abortuses. |
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| Haemoglobin Hasharon in a north Italian community. |
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| The Biology of Racial Integration |
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| 45,X Turner's syndrome in monozygotic twin sisters. |
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| A family with an inherited translocation involving the no. 4/no. 21 chromosomes. |
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| Stub thumbs |
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| Trisomy 4q32 leads to 4qter due to a maternal 4/21 translocation. |
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| Malformation Syndromes |
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| Huntington's Chorea, 1872-1972 |
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| Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring. |
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| Carbohydrate metabolism in dystrophia myotonica. |
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| Genetical components of physiological tremor. |
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| Familial trisomy 7 mosaicism. |
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| Transplacental passage of blood cells. |
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| Development of dermal ridges in the fetus. |
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| Haemoglobin Lepore in Cyprus. |
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| A case of partial (9p) trisomy in a family with a balanced translocation 46,XX,t(1p+9q-). |
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| Practical Human Cytogenetics |
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| Distal brachyphalangy of the thumb in mental retardation. |
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| Trisomy of the short arm of chromosome 10. |
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| HUMAN CYTOGENETIC REGISTRIES |
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| Clinical Cytogenetics and Genetics |
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| Partial 12p deletion: a cause for a mental retardation, multiple congenital abnormality syndrome. |
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| Prenatal diagnosis of a neural tube defect: Meckel syndrome. |
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| Einfuhrung in die Immonogenetik |
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| Psychiatrie. Vol. 8. Die Erblichen Myoklonisch-Epileptische-Dementiellen Kernsyndrome. |
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| Genetic factors in amyloidosis. |
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| The search for relevant cell culture research in cystic fibrosis: one researcher's opinion. |
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| Progress in Medical Genetics, Volume X |
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