| Shorter Notices: Biology and the Social Crisis. A Social Biology for Everyman |
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| Inheritance of tooth size in Liverpool families. |
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| Studies on glucose-6-phosphate dehydrogenase deficient Egyptian families. |
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| Familial jaw cysts in Charcot-Marie-Tooth disease. |
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| Congenital malformations associated with a ring 4 chromosome. |
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| Books and Monographs: Blood Groups in Man |
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| Double autosomal trisomy (trisomy D+G) with mosaicism. |
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| Brachydactyly in an Indian family. |
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✓ |
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Indian family |
| Books and Monographs: The Haptoglobin Groups in Man |
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| Books and Monographs: Cell Function, 2nd Edition |
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| Conductive hearing loss and malformed low-set ears, as a possible recessive syndrome. |
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| Risk factors for coronary heart disease in Hawaiian and Japanese males in Hawaii. |
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| Inheritance of coeliac disease. |
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| XYY syndrome, and XYY-XXYY mosaicism also showing features of Klinefelter's syndrome. |
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| Welshness and fertility. |
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| A haptoglobin Johnson family with nonhypohaptoglobinaemic HpJ-Hp2. |
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| A patient with 45,XX,Gminus-46,XX,Gr mosaicism. |
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| Books and Monographs: Elements of Medical Genetics |
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| Books and Monographs: A Dictionary of Genetics |
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| A family study of atrial septal defect. |
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| E ring chromosome with persistent left superior vena cava and hypertrophic subaortic stenosis. |
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| Chromosome abnormalities in two cases with bilateral radial element defects. |
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| Surveys, Symposia, and Transactions: Strahlengenetik der Sauger, insbesondere der Maus, in ihrer Bedeutung fur das Mutations-problem beim Menschen (Radiation genetics in mammals, particularly in the m |
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| Books and Monographs: Episomes |
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| Surveys, Symposia, and Transactions: Current Topics In Microbiology and Immunology. Vol. 42, Insect Viruses |
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| Risks of offspring of patients with patent ductus arteriosus. |
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| Surveys and Symposia: Cold Spring Harbor Symposia on Quantitative Biology. Vol. XXXII. Antibodies |
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| Shorter Notices: Kraniofaziale Dysplasien und Storungen der Zahnentwicklung Experimentelle und vergleichende Untersuchungen |
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| Corrigendum |
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| ABO and Rh blood groups in relation to blood donors' sibs. |
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| An association of Rh type and gynaecological disease with twinning. |
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| Partial trisomy in a child with features suggesting mongolism. |
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| Books and Monographs: The Congenital Methemoglobinemias. Physiology and Pathophysiology of the Methemoglobin Metabolism |
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| Books and Monographs: Primer of Chromosome Practice. Plant and Animal Chromosomes Under the Microscope |
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| Books and Monographs: Biophysical Technique as Applied to Cell Biology |
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| Evidence of selection in mosaicism. |
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| Ring chromosomes in two infants with congenital malformations. |
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| Books and Monographs: An Inquiry Concerning Growth, Disease and Ageing |
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| Surveys, Symposia, and Transactions: Biomedical Challenges Presented by the American Indian |
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| Surveys, Symposia, and Transactions: Molecular Genetics |
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| Down's syndrome: chromosome analysis in 321 cases in Japan. |
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| Two new cases of true hermaphroditism. |
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| A new mutant gene possibly carried simultaneously by two distinct gametes. |
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| Books and Monographs: Biomathematics. The Principles of Mathematics for Students of Biological and General Science |
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| Books and Monographs: Der gerechtfertigte Haeckel. Einblicke in seine Schriften aus Anlass des Erscheinens seines Hauptwerkes `Generelle Morphologie der Organismen' vor 100 Jahren |
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| Surveys, Symposia, and Transactions: Genetic and Environmental Influences on Behaviour |
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| Surveys, Symposia, and Transactions: Child Care in Health and Disease |
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| Shorter Notices: Genetic Engineering |
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| Inheritance of testicular feminization syndrome: some negative linkage findings. |
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| Clinical and chromosome studies in Fanconi's aplastic anaemia. |
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| Favism: clinical and biochemical data. |
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| Blood cell enzymes in trisomy E (18) syndrome. |
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| Incidence of cleft lip and palate in British Columbia Indians. |
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| Trisomy-16 in a mosaic carrier father and his aborted foetus. |
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| Chromosomal abnormality, megaloblastosis, and arrested DNA synthesis in erythroleukaemia. |
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| Syndrome of retardation with urogenital and skeletal anomalies (Smith-Lemli-Opitz syndrome): clinical features and mode of inheritance. |
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| Consistent and variable chromosome anomalies in parents of children with Down's syndrome. |
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| Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p). |
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| Postaxial polydactyly in three Indian families. |
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| Double autosomal trisomy and mosaicism for three cell lines in man: coexisting trisomy 13-15, trisomy 17-18, and a minority cell line trisomic for a chromosome of both groups. |
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| A patient with a short arm deletion of chromosome 18 (46,XY,18p-). |
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| Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance. |
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| Inhibition of the motility of gill cilia of Dreissensia by plasma of cystic fibrosis patients and their parents. |
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| G6PD deficiency and favism in the island of Rhodes (Greece). |
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| Plasma corticosteroids in healthy twin pairs. |
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| Parental dermotoglyphs in age-independent mongolism. |
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| Multiple congenital anomalies associated with a ring-D chromosome. |
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| Retinoblastoma and deletion D (14) syndrome. |
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| Colonic cancer arising in polyposis coli. |
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| Immunological profile in a chromosome 18 deletion syndrome with IgA deficiency. |
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| A liveborn infant with complete triploidy (69,XXX). |
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| A mentally retarded child convulsions, agenesis of the corpus callosum, and a translocation involving chromosomes 2 and the B group. |
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| Books and Monographs: The Genetics of Bacteria and their Viruses. Studies in Basic Genetics and Molecular Biology |
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| Books and Monographs: Biological Aspects of Cancer and Ageing. Studies in Pure Line Mice |
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| Dominant anonychia and onychodystrophy. |
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| W.M. Court Brown. |
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| Books and Monographs: The Ultrastructure of the Animal Cell |
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| Shorter Notices: Histo- und Zytogenese der sich entwickelnden Retina: Eine elektronenmikroskopische Studie |
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| A prospective, cytogenetic study of recurrent abortion. |
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| Gastric cancer in Wales. |
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| Presumptive C-15 translocation and familial large Y identified by autoradiography. |
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| Hypertrophic pyloric stenosis: adult and congenital types occurring in the same family. |
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| Comparison of strength of isoagglutinin titres in English and Finnish populations. |
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✓ |
|
English and Finnish populations |
| Familial transmission of a chromosomal translocation t(2q+;Cp-). |
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| Blood groups and lung cancer. |
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| 46,XY,21qi-46,XY,21p- mosaicism in a child with Down's syndrome. |
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| Surveys, Symposia, and Transactions: Research in Muscular Dystrophy |
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| Surveys, Symposia, and Transactions: Screening in Medical Care. Reviewing the Evidence |
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| Shorter Notices: Forerunners of Darwin, 1745-1859 |
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| G6PD deficiency in two autochthonous Croatian families. |
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✓ |
|
Croatian |
| Incidence of G6PD deficiency in patients of three different ethnic groups suffering from pulmonary tuberculosis. |
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| Books and Monographs: A Laboratory Manual on Abnormal Haemoglobins |
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| Shorter Notice: Genetics for O Level |
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| Anomalies of chromosome no. 3 in abortuses. |
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| A recessively inherited mixed polyneuropathy of early onset. |
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| Isochromosome for long arm of Y chromosome in patient with Turner's syndrome and sex chromosome mosaicism (45,X-46,XYqi). |
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| Books and Monographs: Selected Topics in Medical Genetics |
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| Books and Monographs: Late Somatic Effects of Ionizing Radiation |
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| Books and Monographs: British Medical Bulletin |
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| Shorter Notices: The Science of Genetics: an Introduction to Heredity |
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| Books and Monographs: Heredity and Environment in the Functional Psychoses. An Epidemiological-Clinical Twin Study. Case Histories |
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| Sex chromatin of hydatidiform moles. |
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| Distribution and heredity of erythrocyte G6PD activity and electrophoretic variants among different racial groups at Sao Paulo, Brazil. |
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✓ |
|
racial groups |
| Oesophageal cancer in Wales. |
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| Hearing impairment in female carriers of the sex-linked syndrome of deafness with albinism. |
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| Mongolism and maternal menarche. |
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| Further evidence for close linkage of the Hb-beta and Hb-delta loci in man. |
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| Books and Monographs: An Atlas of Mammalian Chromosomes |
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| Shorter Notices: Genetische Familienberatung. Ein Leitfaden fur den Artz |
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| Inheritance of congenital pyloric stenosis. |
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| Apple peel syndrome (congenital intestinal atresia): a family study of seven index patients. |
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| A cytogenetic study of familial deafness. |
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| Sjogren-Larsson syndrome in a Turkish family. |
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| Huntington's chorea in a Chinese family. |
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| Books and Monographs: Experiments in Microbial Genetics |
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| Books and Monographs: Clinical Pathology in Mental Retardation |
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| Neonatal intestinal lipidosis in mice. An inherited disorder of the intestinal lymphatic vessels. |
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|
| Occurrence of a presumptive C-B translocation carrier [46,XY,t (? Cp-; Bp+)] in a family of D-G translocation carriers [45,D-,G-,t (DqGq)+]. |
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| An unusual balanced reciprocal translocation in several members of a family. |
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| An improved and simplified method of detecting the acetylator phenotype. |
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| Benign, recessively inherited choreo-athetosis of early onset. |
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| Two cases of trisomy C6-12 mosaicism with multiple congenital malformations. |
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| Books and Monographs: Genetic Markers in Human Blood |
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| Surveys, Symposia, and Transactions: Advances in Immunogenetics |
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| Books and Monographs: Evolutionsprozesse. Einzelvorgange im Wandel der Organismen. Grundbegriffe der modernen Biologie |
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| Congenital extrahepatic biliary atresia in two brothers. |
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| Chromosome 15 abnormality in a mentally retarded adult. |
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| Books and Monographs: Human Developmental Genetics |
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