| Haemoglobin H disease in 2 Filipino families. |
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| Chromosome banding studies in two patients with XXXXY syndrome. |
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| Translocation of chromosome 4 and 9 with ring formation of chromosome 4 short arm. |
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| Computerised chromosome data bank |
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| Developmental Biology and Pathology. (Current Topics in Pathology.) |
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| The Gardner syndrome: a cell culture study on kindred 109. |
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| On the relation between malaria and G-6-PD deficiency: a reply |
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| Down syndrome and recent demographic trends in Manitoba. |
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| Clinical experience with trisomies 18 and 13. |
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| Atlas des Maladies Chromosomiques |
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| Linkage relations of a locus for congenital total nuclear cataract. |
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| First premarital screening of thalassaemia carriers in intermediate schools in Latium. |
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| Number of C-bands of human isochromosome Xqi and relation to 45,X mosaicism |
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| Population heterogeneity in human sperm DNA content. |
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| Epiphysial dysplasia: a constant finding in the XXXXY syndrome. |
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| Heterozygote advantage for the phenylketonuria allele. |
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| Oral Facial Genetics |
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| The Eye in Chromosome Duplications and Deficiencies |
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| Molecular Anthropology. Genes and Proteins in the Evolutionary Ascent of the Primates |
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| Medical Genetics. Proceedings of the Symposium at Debrecen-Hajduszoboszlo, Hungary, 27-29 April, 1976 |
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| Pericentric inversions inv(2)(p11q13) and inv(2)(p13q11) in 2 unrelated families. |
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| 47,XX,+der(18),t(9;18)(p24;q21) mat: a distinct partial trisomy 18q--syndrome? |
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| The phenotype Ae1B: a probable result of chimerism. |
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| Absent left hemidiaphragm, arhinencephaly, and cardiac malformations. |
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| Thalassaemia of intermediate severity resulting from the interaction between alpha- and beta-thalassaemia. |
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| Partial trisomy 6p with karyotype 46,XY,der(22), t(6;22)(p22;q13)mat. |
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| Comment. |
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| Validation and aplication of an interval factor in estimating age at onset of Huntington's disease. |
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| Use of overlapping normal distributions in genetic counselling. |
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| Genetic counseling of consanguineous families. Use of Smith's method to calculate recurrence risks in multifactorial inheritance in consanguineous matings. |
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| Partial trisomy 18 in a family with a translocation (18;21)(q21;q22). |
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| Familial radioulnar synostosis. |
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| Cellular content of amniotic fluid as predictor of central nervous system malformations. |
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| Brachydactyly, distal symphalangism, scoliosis, tall stature, and club feet: a new syndrome. |
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| Acute myelogenous leukaemia in Hurler's syndrome. |
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| Genetic study of narcoleptic syndrome. |
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| Question and answer |
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| Guidelines for Research Involving Recombinant DNA Molecules |
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| Immunology for the Practising Physician |
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| On the relation between malaria and G-6-PD deficiency |
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| Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16. |
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| Apical systolic click and murmur associated with neurofibromatosis. |
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| Placentation, anencephaly, and spina bifida. |
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| Biochemical Methods in Medical Genetics |
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| Errata |
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| Thalassaemia types and their incidence in Sardinia. |
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| Taurodontism and Klinefelter's syndrome. |
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| X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies. |
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| Prenatal diagnosis of a de novo Y/22 translocation. |
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| The Aase syndrome in a female infant. |
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| Supernumerary small ring chromosome. |
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| Genetic family history questionnaire |
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| E1k, another quantitative variant at cholinesterase locus 1. |
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| Raised alpha-fetoprotein levels in amniotic fluid and maternal serum associated with distension of the fetal bladder caused by absence of urethra. |
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| Primary hypogonadism in the Borjeson-Forssman-Lehmann syndrome. |
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| Partial 18 trisomy (with 47 chromosomes) resulting from a familial maternal translocation. |
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| Medico-Social Management of Inherited Metabolic Disease |
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| Shifting genetic patterns in anencephaly and spina bifida. |
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| Unusual inheritance of Becker type muscular dystrophy. |
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| Recessively inherited costovertebral segmentation defect with mesomelia and peculiar facies (Covesdem syndrome): A new genetic entity? |
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| Fertility in 47,XXX and 45,X patients. |
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| Partial trisomy for short and long arm of chromosome no. 5: Two cases of two possible syndromes. |
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| Erythropoietic protoporphyria, heterozygous cystinuria, and reduced peptidase A activity in a patient with 46,XX/46,XX,18q--mosaicism. |
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| A family study of vesicoureteric reflux |
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| Parthenogenesis. |
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| Hereditary pancreatitis in England and Wales. |
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| Nephrogenic diabetes insipidus and Werdnig-Hoffmann disease in a child: an unusual association. |
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| Late discovery of a case of testicular feminisation. |
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| Calculation of genetic risks in Duchenne muscular dystrophy by geneticists in the United Kingdom. |
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| Combined use of alphafetoprotein and amniotic fluid cell morphology in early prenatal diagnosis of fetal abnormalities. |
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| Length heteromorphisms of fluorescent (f) and non-fluorescent (nf) segments of human Y chromosome: classification, frequencies, and incidence in normal Caucasians. |
✓ |
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| Bilateral renal agenesis in 2 male sibs born to consanguineous parents. |
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| Neural tube defects in New South Wales, Australia |
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| Estimation of proportion of new mutants among cases of Duchenne muscular dystrophy. |
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| Familial atypical multiple mole-melanoma syndrome. |
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| Segregation of an insertional chromosome rearrangement in 3 generations. |
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| Trisomy 21 with 47,+18 lymphocyte cell line: double mitotic nondisjunction. |
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| Triplication of a short arm region of chromosome 15. |
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| Reproduction in a woman with mosaicism. |
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| Osteosarcoma in a patient with Hutchinson-Gilford progeria. |
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| Predisposition to spina bifida. |
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| Risk of coeliac disease in children of patients and effect of HLA genotype. |
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| Waardenburg-like features with cataracts, small head size, joint abnormalities, hypogonadism, and osteosarcoma. |
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| Trisomy 8 syndrome. |
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| Down's Anomaly 2nd ed |
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| Chemical Mutagens. Principles and Methods for their Detection Vol. 4 |
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| Advances in Human Genetics. Vol. 7 |
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| Hereditary brachydactyly with nail dysplasia. |
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| De novo simultaneous reciprocal translocation and deletion. |
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| Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome. |
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| Autosomal recessive postaxial polydactyly type A in a Sicilian family. |
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| Linkage studies in Van der Woude syndrome. |
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| Necropsy of original case of Lowry's syndrome. |
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| Inconsistent expression of both centromeres of a dicentric Y chromosome in a child with ambiguous external genitalia. |
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| Linkage analysis in dominant acrocephalosyndactyly. |
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| Myotonia Congenita and Syndromes Associated with Myotonia. Clinical-Genetic Studies of the Nondystrophic Myotonias |
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| Introduction to Biometrical Genetics |
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| Clinics in Rheumatic Diseases, Vol. 3, No. 2. Immunogenetics and Rheumatic Disease |
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| Le Polymorphisme Biochimique et Les Facteurs de Son Maintien |
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| Incidence, prevalence, and gene frequency studies of chronic childhood spinal muscular atrophy. |
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| Genetics of adolescent idiopathic scoliosis. |
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| A report on genetic registers. Based on the report of the Clinical Genetics Society Working Party. |
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| Report of a mucopolysaccharidosis occurring in Australian aborigines. |
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| Simplified classification of spontaneous abortions. |
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| The Axenfeld syndrome and the Rieger syndrome. |
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| Trisomy 18 syndrome with an unusual karyotype: possible double isochromosome. |
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| Principles of Genetic Counselling |
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| Population Cytogenetics: Studies in Humans |
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| A new type of chondrodystrophic mutant in the mouse. |
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| Significance of detection of extra metacentric microchromosome in amniotic cell culture. |
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| Cleft palate and accessory metacarpal of index finger syndrome: possible familial occurrence. |
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| Inducibility of aryl hydrocarbon hydroxylase in cultured human lymphocytes: a study of repeatability. |
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| Deletion 14q and pericentric inversion 14. |
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| Meckel's syndrome (dysencephalia splanchno-cystica) in two Pakistani sibs. |
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| Training of medical geneticists. |
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| Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family. |
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| Family studies of relation between Perthes disease and congenital dislocation of the hip |
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| Complete trisomy 5p |
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| Dominance in human genetics. |
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| Oral Manifestations of Inherited Disorders |
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| Gene-Environment Interaction in Common Diseases. Proceedings of the Symposium on Gene-Environment Interaction in Common Diseases held February 11-12, 1976, Tokyo |
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| Spontaneous regression of metastatic malignant melanoma in 2 sibs with xeroderma pigmentosum. |
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| A new form of Niemann-Pick disease characterised by temperature-labile sphingomyelinase. |
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| Genetic studies of acute infantile spinal muscular atrophy (SMA type I). An analysis of sex ratios, segregation ratios, and sex influence. |
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| Segregation analysis of chronic childhood spinal muscular atrophy. |
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| Angiokeratoma corporis diffusum (Anderson-Fabry disease) in a single large family in Nova Scotia. |
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| Meckel syndrome and the prenatal diagnosis of neural tube defects. |
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| A 'new' syndrome of mental retardation with characteristic facies and brachyphalangy. |
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| Popliteal pterygium syndrome: a phenotypic and genetic analysis. |
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| Experimental Biology and Medicine Cytogenetic aspects of Malignant Transformation |
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| Dermatoglyphics in Medical Disorders |
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| Heterozygote advantage for the phenylketonuria allele. |
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| Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q). |
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| The Marden-Walker syndrome. |
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