| Conenital hypothyroidism in association with a ring chromosome 18. |
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| Chemical Mutagenesis in Mammals and Man |
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| Lionel Sharples Penrose (1898-1972), MA,MD,DSc,FRCP,FRS. |
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| 46,Xinv(Yp+q-) in four generations of an Indian family. |
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| Unstable haemoglobin Koln disease in members of a Malay family. |
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✓ |
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Malay |
| Genetical, Functional, and Physical Studies of Hemoglobins |
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| Trisomy G/Normal Mosaicism. A Cytological and Clinical Investigation |
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| Reciprocal chromosome translocations: analysis of two mutants by interactive computer. |
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| The nature and inheritance of Kirner's deformity. |
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| The effect of absence of thumb on palmar dermatoglyphics. |
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| The Role of Genetics in Mental Retardation |
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| Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques. |
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| The Genetics of Mental Disorders |
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| Papers on Regulation of Gene Activity During Development |
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| The incidence and genetics of cystic fibrosis. |
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| The value of investigations of the incidence of peptic ulcer in the families of patients with duodenal ulcer. |
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| Development of humoral and cellular immunity in man. |
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| Mongolism and sex: a common problem of cell proliferation? |
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✓ |
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Mongolism |
| A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome. |
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| Blood enzymes in the de Lange syndrome. |
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| Congenital absence of the fibula and craniosynostosis in sibs. |
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| Ecological Genetics and Evolution |
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| Giemsa banding pattern of a heritable 1q+ variant chromosome: a possible partial duplication. |
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| Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-). |
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| Immunoglobulin abnormality in a girl with a large chromosome 18. |
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| A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother. |
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| A rare blood group antigen An a (Ahonen). |
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| Erythrocyte acid phosphatase polymorphism and haemolysis. |
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| Familial cancer of the colon and rectum. |
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| Comparative Genetics in Monkeys, Apes and Man |
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| Inherited pericentric inversion of a group D (13-15) chromosome. |
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| A 45,XX,21--child: attempt at a cytological and clinical interpretation of the karyotype. |
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| True hermaphroiditism: cytogenetic analysis, surgical repair, and social implications. |
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| Two cases of trisomy D associated with adrenal tumours. |
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| Nystagmus in a female carrier of ocular albinism. |
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| Birth Defects: Original Article Series, VII, 1 |
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| Genetical investigations in dyslexia. |
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| Antinuclear factor in rapid and slow acetylator patients treated with isoniazid. |
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| The use of the autoanalyzer to determine the acetylator phenotype. |
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| A syndrome of mental and physical etardation, speech disorders, and peculiar facies in two sisters. |
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| Camurati-Engelmann disease. Genetics and clinical manifestations with a review of the literature. |
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| A family study of Fallot's tetralogy. |
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| Camptodactyly: occurrence in two new genetic syndromes and its relationship to other syndromes. |
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| Recessively inherited myotonia congenita. |
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| A case of double aneuploidy, 47,XXY,14-,t(13q14q)+, also probably homozygous for the cystic fibrosis gene. |
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| Immunological studies in congenital nephrosis. |
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| Corrigenda |
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| Antenatal development of amylase isoenzymes. |
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| The inheritance of dental traits in a Chinese population in the United Kingdom. |
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| A Psychological-Psychiatric Study of Patients with Klinefelter's Syndrome, 47,XXY |
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| Diagnosis of Metabolic Eye Diseases |
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| A new genetic variant of the spinal muscular atrophies in infancy. |
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| Haemoglobin Q India (alpha 64(E13) aspartic acid histidine) associated with beta-thalassemia observed in three Sindhi families. |
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| Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography. |
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| Congenital leukaemia with 46,XX,t(Bq+,Cq-) cells. |
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| Turner's syndrome with menstruation. |
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| A Duarte variant with clinical signs. |
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| A twin study of the genetic influences on the electroencephalogram. |
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| Autosomal dominant inheritance and amino aciduria in Blackfan-Diamond anaemia. |
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| The autosomal recessive variety of congenital stationary night-blindness with myopia. |
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| Twin heritability study of the effect of corticosteroids on intraocular pressure. |
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| ABO incompatibility as a cause of spontaneous abortion: evidence from abortuses. |
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| Rural-urban differentials in consanguinity. |
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| Incidence and genetics of Legg-Perthes disease (osteochondritis deformans) in British Columbia: evidence of polygenic determination. |
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| Triple X female and a Down's syndrome offspring. |
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| Double aneuploidy (47,XX,21+-45,X) arising through simultaneous double non-disjunction. |
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| Corrigenda |
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| Gene duplication, mutation load, and mammalian genetic regulatory systems. |
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| The use of new staining techniques for human chromosome identification. |
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| Cytogenetic survey of XYY males in two juvenile court populations, with a case report. |
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| Genetic heterogeneity for dystrophia myotonica. |
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| Dominant ectrodactyly and possible germinal mosaicism. |
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| X-linked mental retardation without physical abnormality (Renpenning's syndrome) in sibs in an institution. |
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| Superior intelligence in sighted retinoblastoma patients and their families. |
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| Genetic aspects of selective immunoglobulin A deficiency. |
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| Normal male development with Y chromosome long arm deletion (Yq-). |
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| A ring-20 chromosome. |
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| The Genetics of Human Populations |
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| Bibliographica genetica medica |
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| Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals. |
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| Palmar dermatoglyphs in tuberous sclerosis. |
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| Bone marrow chromosomes in Fanconi's anaemia. |
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| Down's syndrome with an atypical G-G translocation derived from familial pericentric inversion in one chromosome of the G group. |
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| Biomathematics |
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| Molecular Genetics. An Introductory Narrative |
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| Probability Models and Statistical Models in Genetics |
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| Pyloric atresia. A hereditary congenital anomaly with autosomal recessive transmission. |
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| Haemoglobin Ocho Rios ( beta52 (D3) aspartic acid leads to alanine): a new beta-chain variant of haemoglobin A found in combination with haemoglobin S. |
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| A new G-6-PD variant associated with chronic non-spherocytic haemolytic anaemia in a negro family. |
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✓ |
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negro |
| The polymorphic acetylation of sulphapyridine in man. |
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| Syndrome of pigmentary retinal degeneration, cataract, microcephaly, and severe mental retardation. |
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| A case of 48,XXXX female with normal intelligence. |
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| Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism. |
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| Multiple congenital defects associated with an abnormal unclassifiable karyotype. |
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| Cri-du-chat syndrome combined with partial C-group trisomy. |
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| A sex chromatin study of Chinese school children. |
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| Familial chronic muco-cutaneous candidiasis. |
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| 48,XYYY: a new syndrome? |
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| A double aneuploid mosaic: trisomy 13 and XXY. |
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| Immunogenetics |
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| Pedigrees with diabetes insipidus, diabetes mellitus, and optic atrophy. |
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| Ring F chromosome mosaicism (46,XY,20r-46,XY) in an epileptic child without apparent haematological disease. |
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| Fanconi's anaemia: report of a patient with significant chromosomal abnormalities in bone marrow cells. |
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| A new HGPRT-deficient phenotype? |
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| Deletion of the long arms of chromosome 18 (46,XX,18q-) associated with absence of IgA and hypothyroidism in an adult. |
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| Coefficients of Natural Selection |
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| Cytoenzymology and Isozymes of Cultured Cells |
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| Hereditary Sensory Radicular Neuropathy |
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| Genes, Dreams and Realities |
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| A statistical study of half-sibships born to parents affected with Huntington's disease. |
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| Familial correlations for age at onset and age at death in Huntington's disease. |
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| Variation in secretor and Lewis type frequencies within the British Isles. |
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| ABH secretor and Lewis type frequencies in an Icelandic series. |
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| Abnormalities of the electrocardiogram in hereditary myopathies. |
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| Serum iron and unsaturated iron-binding capacity in the -thalassaemia trait: their relation to the levels of haemoglobins A, A 2 , and F. |
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| Searching for XYY males through electrocardiograms. |
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| A human ring C chromosome associated with multiple congenital abnormalities. |
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| Messenger RNA in animal cells. |
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| Early Diagnosis of Human Genetic Defects--Scientific and Ethical Considerations |
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| The Dombrock system: linkage relations with other blood group loci. |
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| Christmas disease in one of a pair of monozygotic twin girls, possibly the effect of lyonization. |
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| Apparent G-monosomy, G-deletion, and incomplete Down's syndrome in a single family. |
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| Progress in Medical Genetics, Vol. 8 |
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| The dominant and recessive forms of cutis laxa. |
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| Popliteal pterygium syndrome. Evidence for a severe autosomal recessive form. |
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| Correspondence |
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| The Bacteriophage Lambda |
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| Addendum |
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| Aminoacidopathies, Immunoglobinopathies, Neuro-genetics and Neuro-ophthalmology |
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