| Atlas of Mental Retardation Syndromes. Visual Diagnosis of Facies and Physical Findings |
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| Severe achondroplasia: demonstration of probable heterogeneity within this clinical syndrome. |
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| Prevalence of abnormal haemoglobins in pulmonary tuberculosis in three different ethnic groups. |
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| Developmental abnormalities in a patient with karyotype 46,XX,bq+. |
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| The Elements of Cytogenetics |
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| L'heredite du glaucome a angle ouvert. |
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| Choroidal atrophy. Clinical and genetic types. |
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| Reflections on abnormal colour vision and theories of colour. |
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| Endocrine and Genetic Diseases of Childhood |
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| Fortschritte der allegemeinen und klinischen Humangenetik |
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| Adenosine deaminase: racial distribution and report of a new phenotype. |
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| Affected parent and age of onset in Huntington's chorea. |
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| Down's syndrome and acute leukaemia: a cytogenetic study. |
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| A 46,XX,t(Cp+;Cq-) translocation in a girl with multiple congenital anomalies and in her phenotypically normal father 46,XY,t(Cq+;Cq-). |
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| A female with the 48,XXXX karyotype. |
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| A 45,XY,5-15-,t(5q15q) cri-du-chat child. |
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| Uveal coloboma and true Klinefelter syndrome. |
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| Hereditary macular coloboma. |
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| Eyes on chromosomes. |
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| A Study of the Early Development of Mongols. Institute for Reasearch into Mental Retardation Monograph No. 1 |
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| Human Blood and Serum Groups |
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| Value of butyrylthiocholine assay for identification of cholinesterase variants. |
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| Gonadoblastoma in a phenotypic female with 45,X-47,XYY mosaicism. |
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| Evolution and the Genetics of Populations. A Treatise in Three Volumes. Volume 2: The Theory of Gene Frequencies |
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| Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome. |
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| Congenital adrenal hypoplasia--an X-linked disease. |
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| ABO blood groups, haemoglobin genotypes, and loiasis. |
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| Trisomy E and T-E fistula. |
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| 48,XY,21+, mar+mat: a case of trisomy 21 associated with an inherited small marker chromosome. |
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| Relation of face shape to susceptibility to congenital cleft lip. A preliminary report. |
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| Trisomy 13 syndrome in Chinese infants. Clinical findings and incidence. |
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✓ |
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Chinese infants |
| Familial occurrence of a small, supernumerary metacentric chromosome in phenotypically normal women. |
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| Familial hypertrichosis cubiti: hairy elbows syndrome. |
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| Hemifacial microsomia--oculo-auriculo-vertebral dysplasia. A patient with overlapping features. |
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| Progress in Medical Genetics |
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| Gene Activity in Early Development |
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| Tapeto-retinal degenerations with varying clinical features in Aland islanders. |
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| Les manifestations oculaires des malaides par aberrations des chromosomes non sexuels. |
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| Genetic Load. Its Biological and Conceptual Aspects |
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| Editorial |
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| A family study of neonatal and late-diagnosis congenital dislocation of the hip. |
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| Comments on patients with sex chromosome aneuploidy: dermatoglyphs, parental ages, Xg a blood group. |
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| D1 ring chromosome in newborn with peculiar face, polydactyly, imperforate anus, arrhinencephaly, and other malformations. |
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| Genetic Counseling. A Guide for the Practicing Physician |
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| A deleted B chromosome in a mosaic mother and her cri du chat progeny. |
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| A family with a large Y chromosome. |
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| Huntington's chorea. Report of a chinese family in Singapore. |
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✓ |
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chinese |
| Thalassaemia intermedia: a genetic study in 11 patients. |
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| New human double trisomy or tetrasomy. |
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| t(2q-; Dq+) in a mentally retarded female child. |
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| Von Hippel-Lindau syndrome: a report on three kindreds. |
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| Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4. |
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| Deletion of short arm of no. 4 (4p-)--a detailed case report. |
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| Grundriss der Genetik |
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| Some notes on publications of Professor Arnold Sorsby and on Aland eye disease (Forsius-Eriksson syndrome). |
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| Bassen-Kornzweig syndrome. Present status. |
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| Biochemistry of retinal dystrophy. |
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| Fluorescence angiography and inherited degeneration of the fundus oculi. |
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| Biochemical Methods in Red Cell Genetics |
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| The Handling of Chromosomes |
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| Ophthalmic Genetics |
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| Genetics of immunity deficiency syndromes. |
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| Dermatoglyphs of Chinese children and Down's syndrome. |
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| An extra chromosomal centric fragment in an infant with stigmata of Down's syndrome. |
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| Cold Spring Harbor Symposia on Quantitative Biology, Vol. XXXIV |
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| The Future of the Brain Sciences. Proceedings of a Conference held at the New York Academy of Medicine, May 2-4, 1968 |
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| Some Inherited Disorders of Brain and Muscle. Proceedings of the Fifth Symposium of the Society for the Study of Inborn Errors of Metabolism |
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| ABO and Rh blood groups in relation to marital status and childlessness in blood donors. |
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| Inherited pericentric inversion of a human Y chromosome in trisomic Down's syndrome. |
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| Autosomal deletion syndrome 46,XX,18p-: a new case report with absence of IgA in serum. |
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| Chromosome abnormalities in early spontaneous abortions. |
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| Dermatoglyphs in leukaemia. |
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| Recessive albinism in three children and both parents. |
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| Familial occurrence of congenital malformations and ring chromosome (46,XX,Cr). |
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| The Chromosome Disorders. An Introduction for Clinicians |
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| Human Afflictions and Chromosome Abberations |
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| Chromosomes and Genes. The Biological Basis of Heredity |
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| Genetics of closed-angle glaucoma. |
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| Hereditary nystagmus in early childhood. |
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| An Introduction to Medical Genetics |
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| Haemoglobin J in the French Canadian. |
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✓ |
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French Canadian |
| Trisomy E (18) syndrome: clinical spectrum in 12 new cases, including chromosome autoradiography in 4. |
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| Protease inhibitor (Pi) phenotypes in chromosome aberrations. |
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| A rare translocation (47,XY,t(2p-;21q+),21+) associated with Down's syndrome. |
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| A case of XX male syndrome. |
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| Cytogenetic studies in a patient with a de novo t(Cq-;Gp+). |
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| An unusual chromosomal aberration in a case of Chediak-Higashi syndrome. |
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| The Biology of Twinning in Man |
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| Humangenetik. Ein kurzes Handbuch in funf Banden |
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| Progress in Human Behaviour Genetics: Recent Reports on Genetic Syndromes, Twin Studies, and Statistical Advances |
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| Genetics and Counseling in Medical Practice |
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| Chromosomale Aberrationen und Psyche |
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| Modern Biology |
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| Absent IgA and deletions of chromosome 18. |
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| Genetic factors influencing human serum trehalase activity. |
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| Achondroplasia and Down's syndrome. |
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| Median facial cleft associated with ring E chromosome. |
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| Familial XY gonadal dysgenesis. |
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| Trisomy 18 syndrome in Chinese infants. Clinical findings and incidence. |
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✓ |
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Chinese |
| Significance of chromosome 17ps+ in three generations of a family. |
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| Nucleic Acid Metabolism Cell Differentiation and Cancer Growth: Proceedings of the second international symposium for cellular chemistry |
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| Endocrinopatile Genetice |
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| Genetical aspects of severe visual impairment in childhood. |
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| Some problems in population genetics. |
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| Animal models for bone-marrow transplantation. |
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| Mutation rate in Duchenne type of muscular dystrophy. |
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| A familial syndrome of short stature, deformities of the hands and feet, and an unusual facies. |
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| Evidence of XX-XY sex chromosome mosaicism in a child with true hermaphroditism. |
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| Possible X-autosomal translocation in a girl with gonadal dysgenesis. |
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| Diagnosis and Treatment of Fetal Disorders |
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| Satellite associations of D group chromosomes in translocation carriers. |
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| Normal chromosomes in mucosol neuroma variant of medullary thyroid carcinoma syndrome. |
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| Gargoylism in a Chinese boy. |
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✓ |
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Chinese |
| Elements de Genetique Generale et Humaine |
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