| Presumptive 46,XX-46,XY-47,XXY mosaicism in a hermaphrodite. |
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| Clinical Genetics: An International Journal of Genetics in Medicine |
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| Medizinische Genetik. Grundlagen, Ergebnisse und Probleme |
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| Ahaptoglobinaemia and predisposition to iron-deficiency anaemia. |
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| Double heterozygosity for glucose-6-phosphate dehydrogenase deficiency. |
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| Correspondence |
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| Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance. |
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| Distribution of ABO blood groups, G6PD deficiency, and abnormal haemoglobins in leprosy. |
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| Rh immunization following incompatible blood transfusion and a possible long-term complication of anti-D immunoglobulin therapy. |
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| The Post-natal Development of Phenotype |
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| Klassische und Molekulare Genetik |
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| Genetic Counselling |
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| Cold Spring Harbor Symposia on Quantitative Biology, Vol. XXXV |
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| A case of 47,XX,(21q-)+ with some stigmata of Down's syndrome and an IQ of 77. |
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| Developmental Processes in Higher Vertebrates |
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| Trisomy of chromosome 16 in a neonate, 47XY,?16+. |
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| Methoden in der medizinischen Cytogenetik |
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| The genetic basis of variation in factor 8 levels among haemophiliacs. |
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| Genetic studies on hypospadias in males. |
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| Virilizing adrenal carcinoma in two sibs. |
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| Chromosomal aberrations induced by T strains mycoplasmas. |
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| A family with balanced translocation, t(5p-;Gp+). |
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| Ring 13 chromosome with normal haptoglobin inheritance. |
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| The use of quinacrine fluorescence in the identification of B and E group chromosomes involved in structural abnormalities. |
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| Epidemiology of Mongolism |
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| An ABC of Medical Genetics |
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| Mutation rate in Duchenne muscular dystrophy. |
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| X chromosome long arm deletion in a patient with Down's syndrome. |
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| Genetic Epistemology |
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| The X-linked blood group system Xg. Tests on unrelated people and families of northern European ancestry. |
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✓ |
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northern European ancestry |
| Polymorphism and protein evolution. The neutral mutation-random drift hypothesis. |
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| The nosology of the spinal muscular atrophies. |
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| Origin of sex chromosome monosomy in man. |
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| Phenylketonuria. |
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| Genetic control of nortriptyline kinetics in man: a study of relatives of propositi with high plasma concentrations. |
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| Di Guglielmo syndrome in a t(DgDg) heterozygote. |
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| Birth Defects: Original Article Series, V, 2 |
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| Familial total anomalous pulmonary venous return. |
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| Trisomy D-trisomy E mosaicism in an infant male. |
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| Carcinoma of the breast and Klinefelter's syndrome. |
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| On the pathogenesis of favism. |
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| Simple anonychia. Further evidence for autosomal recessive inheritance. |
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| Essentials of Medical Genetics |
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| Concordance for amyotrophic lateral sclerosis in a pair of dizygous twins of consanguineous parents. |
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| Congenital cleft lip. A genetic study of 496 propositi. |
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| Familial incidence of cerebrovascular disease. |
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| Genetics of childhood spinal muscular atrophy. |
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| 47,XX,13+ with Snodgrass phenotype II. Are different chromosomes associated with two clinical varieties of D-trisomy? |
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| Mental retardation, unusual facies, and abnormal nails associated with a group-G ring chromosome. A case report on two unrelated cases. |
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| A group-C ring chromosome in a mentally deficient male. |
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| A child with a ring G chromosome (46,XX, Gr). |
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| Birth Defects: Original Article Series, V, 3 |
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| Differentiation of two genetically specific types of depression by the response to antidepressant drugs. |
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| Suppression of the immune response. |
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| Group G deletion syndromes. |
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| The inheritance of a structural anomaly of one chromosome No. 16 in a kindred (46,16-,C+). |
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| Partial deletion of a group-F (19-20) chromosome in a physically handicapped psychiatric male patient. |
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| An extra small metacentric autosome in a mentally retarded boy with multiple malformations. |
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| Birth Defects; Original Article Series, V. 4 |
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| Advances in Twin Studies |
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| An analysis procedure illustrated on a triple linkage of use for prenatal diagnosis of myotonic dystrophy. |
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| Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion. |
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| -glucuronidase activity in fibroblasts cultured from persons with and without cystic fibrosis. |
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| Individuals at risk in families with genetic disease. |
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| Abnormal distribution of ABO blood groups in infantile pyloric stenosis. |
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| Monosomy G: case report and review of the literature. |
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| Autosomal translocation in a mentally retarded male child with 46,XY,t(2q-;13q+) complement. Case report and review. |
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| A family showing transmission of a translocation t(3porq-;Cq+). |
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| A 47,XXq-Y Klinefelter male. |
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| Genetics of the Evolutionary Process |
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| Asphyxiating thoracic chondrodystrophy. Association with renal disease and evidence for possile heterozygous expression. |
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| Ovum Implantation: Its Hormonal, Biochemical, Neurophysiological and Immunological Bases |
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| Corrigendum |
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| An inherited kidney disease of mice resembling human nephronophthisis. |
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| Chromosome surveys in penal institutions and approved schools. |
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| Chromosome studies in 101 mentally handicapped Jamaican children. |
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| Gene deletion and duplication effects on phenotype and gamma globulin levels. |
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| A familial variant of chromosome 9. |
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| A case of XYY Down's syndrome confirmed by autoradiography. |
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| 49,XXXXY chromossomal anomaly in a neonate. |
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| The De Lange Syndrome |
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| Polycystic disease of kidney and liver presenting in childhood. |
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| X-linked spondyloepiphyseal dysplasia tarda: clinical and linkage data. |
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| A prisoner with an unusual karyotype (46,XY,Dq-). |
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| An extra small metacentric chromosome in association with multiple congenital abnormalities. |
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| Genetic Concepts and Neoplasia |
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| Elements of Medical Genetics |
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| Congenital hypothyroidism and hyperthyroidism in monozygotic twin girls. |
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| A patient with 45,X-46,XXq--46,XXq-dic karyotype. |
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| A partial D-trisomy-normal mosaic female. |
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| A case of 48,XXY,21+ in an infant with Down's syndrome. |
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| An inherited 1;G translocation. |
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| The 'law of ancestral heredity' and the Mendelian-ancestrian controversy in England, 1889-1906. |
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| Correspondence |
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| Genetic-epidemiological studies in progressive muscular dystrophy. |
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| Chromosome studies in selected spontaneous abortions. Polyploidy in man. |
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| Fertility in balanced heterozygotes for a familial centric fusion translocation, t(DgDg). |
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| A complex chromosomal rearrangement with formation of a ring 4. |
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| Additional G-like chromosome in a malformed boy. |
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| Alzheimer's Disease and Related Conditions |
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| Haemoglobin Osu-Christiansborg: a new beta-chain variant of haemoglobin A ( beta52 (D3) aspartic acid leads to asparagine) in combination with haemoglobin S. |
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| The 13q- deletion syndrome. |
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| Somatic stigmata of Turner's syndrome in a patient with 46,XXq-. |
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| A case of cri-du-chat associated with cataracts and transmitted from a mother with a 4-5 translocation. |
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| Trisomy 18 in one of fraternal twins. |
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| Human Genetics and Medicine |
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| Xg groups and sex abnormalities in people of northern European ancestry. |
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✓ |
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northern European ancestry |
| On the distribution of phenotypes in XXY males and their parents. |
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| ABH secretor status of the fetus: a genetic marker identifiable by amniocentesis. |
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| A ring-4 chromosome in a patient with normal intelligence and short stature. |
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| Additional evidence of gradual loss of germ cells in the pathogenesis of streak ovaries in Turner's syndrome. |
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| The Distribution of the Blood Groups in the United Kingdom |
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| Serendipity in St. Helena. A Genetical and Medical Study of an Isolated Community |
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| Corrigendum |
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| Klinefelter's syndrome and G trisomy. |
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| Remarkable Facts in Human Albinism and Leukism |
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