Published in J Med Genet on August 01, 1983
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Changing incidence and geographical distribution of malignant paediatric germ cell tumours in the West Midlands Health Authority region, 1957-92. Br J Cancer (1995) 0.86
Patterns of childhood cancer among siblings. Br J Cancer (1996) 0.86
Report of fertility in a woman with a predominantly 46,XY karyotype in a family with multiple disorders of sexual development. J Clin Endocrinol Metab (2007) 0.78
High resolution of human chromosomes. Science (1976) 5.56
Non-inactivation of an x-chromosome locus in man. Science (1979) 2.74
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223. Hum Genet (1980) 1.87
Genetically determined sex-reversal in 46,XY humans. Science (1978) 1.76
Association of the H-Y male antigen with beta2-microglobulin on human lymphoid and differentiated mouse teratocarcinoma cell lines. J Exp Med (1978) 1.38
Topological classification of palmar dermatoglyphics. J Ment Defic Res (1970) 1.33
A human quantitative polymorphism related to Xg blood groups. Nature (1981) 1.19
Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data. Birth Defects Orig Artic Ser (1971) 1.05
Familial syndrome of streak gonads and normal male karyotype in five phenotypic females. N Engl J Med (1970) 1.03
XY gonadal dysgenesis and the H-Y antigen. Report on 12 cases. Hum Genet (1979) 0.95
XY gonadal dysgenesis: genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis. Hum Genet (1981) 0.94
Neoplasms of dysgenetic gonads. Am J Obstet Gynecol (1966) 0.88
High resolution banding of prometaphase chromosomes. Hum Genet (1982) 0.85
Familial XY gonadal dysgenesis. J Med Genet (1970) 0.82
Turner syndrome patients are H-Y positive. Hum Genet (1980) 0.81
Prepubertal XY gonadal dysgenesis. Pediatrics (1977) 0.80
X-linked genes of the H-Y antigen system in the wood lemming (Myopus schisticolor). Hum Genet (1982) 0.80
Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell (1994) 7.39
Evolution from fish to mammals by gene duplication. Hereditas (1968) 3.95
Cot deaths in Birmingham 1958-61. Med Sci Law (1965) 2.81
Neuroblastoma in Europe: differences in the pattern of disease in the UK. SENSE. Study group for the Evaluation of Neuroblastoma Screening in Europe. Lancet (1998) 2.77
Altered synaptic physiology and reduced susceptibility to kainate-induced seizures in GluR6-deficient mice. Nature (1998) 2.72
The inter-regional epidemiological study of childhood cancer (IRESCC): a case control study of aetiological factors in leukaemia and lymphoma. Arch Dis Child (1987) 2.49
Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function. Curr Biol (2000) 2.46
[Deficiency on the short arms of a chromosome No. 4]. Humangenetik (1965) 2.46
Inner ear defects induced by null mutation of the isk gene. Neuron (1996) 2.34
Consensus scoring: A method for obtaining improved hit rates from docking databases of three-dimensional structures into proteins. J Med Chem (1999) 2.11
Allele-specific expression and total expression levels of imprinted genes during early mouse development: implications for imprinting mechanisms. Genes Dev (1995) 2.03
Adjuvant low dose radiation in childhood T cell leukaemia/lymphoma (report from the United Kingdom Childrens' Cancer Study Group--UKCCSG). Br J Cancer (1984) 1.97
Is the risk of cancer increased in Asians living in the UK? Arch Dis Child (1994) 1.79
Binomial cokriging for estimating and mapping the risk of childhood cancer. IMA J Math Appl Med Biol (1998) 1.77
A promoter that drives transgene expression in cerebellar Purkinje and retinal bipolar neurons. Science (1990) 1.76
Carcinoid tumours of the appendix in children 1957-1986: incidence, treatment and outcome. Br J Surg (1993) 1.71
Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting. Genes Dev (1995) 1.70
Divided right ventricle: a review of its anatomical varieties. Pediatr Cardiol (1985) 1.65
Clinical significance of antenatal calyceal dilatation detected by ultrasound. Lancet (1990) 1.64
Expression and methylation of imprinted genes during in vitro differentiation of mouse parthenogenetic and androgenetic embryonic stem cell lines. Development (1994) 1.63
Dosimetry of the cone beam computed tomography Veraviewepocs 3D compared with the 3D Accuitomo in different fields of view. Dentomaxillofac Radiol (2008) 1.63
Facts for teachers of children with cancer. Arch Dis Child (1988) 1.61
Evaluation of eight and a half years of neonatal screening for haemoglobinopathies in Birmingham. Br Med J (Clin Res Ed) (1988) 1.59
Sickle cell haemoglobinopathies in England. Arch Dis Child (1981) 1.52
Colonic perforation after exchange transfusion. Br Med J (1968) 1.50
[Monitoring multiple cardiovascular paramaters using telemedicine in patients with chronic heart failure]. Herzschrittmacherther Elektrophysiol (2005) 1.48
Neuroblastoma--when are urinary catecholamines and their metabolites 'normal'? Ann Clin Biochem (1988) 1.48
Establishment, characterization and fibre outgrowth of isolated bovine adrenal medullary cells in long-term cultures. Neuroscience (1980) 1.48
Meckel's diverticulum: its association with congenital malformation and the significance of atypical morphology. Br J Surg (1980) 1.48
Duodenal atresia: a comparison of three modes of treatment. Eur J Pediatr Surg (1996) 1.43
Copper metabolism in mottled mouse mutants: copper concentrations in tissues during development. Biochem J (1979) 1.42
Partial or near-total pancreatectomy for nesidioblastosis? Eur J Pediatr Surg (1995) 1.41
Financial burden of childhood cancer. Br Med J (Clin Res Ed) (1982) 1.41
Poor prognosis of acute lymphoblastic leukaemia in Asian children living in the United Kingdom. Br Med J (Clin Res Ed) (1983) 1.38
Neonatal screening for sickle haemoglobinopathies in Birmingham. Br Med J (Clin Res Ed) (1982) 1.37
Copper metabolism in mottled mouse mutants: copper therapy of brindled (Mobr) mice. Biochem J (1979) 1.36
Bisulfite sequencing in preimplantation embryos: DNA methylation profile of the upstream region of the mouse imprinted H19 gene. Genomics (1998) 1.36
[Crying cat syndrome with translocation 5/D 2]. Humangenetik (1966) 1.35
Childhood cancer in the West Midlands: incidence and survival, 1980-1984, in a multi-ethnic population. Clin Oncol (R Coll Radiol) (1992) 1.33
Parenteral nutrition-related cholestasis in postsurgical neonates: multivariate analysis of risk factors. J Pediatr Surg (1996) 1.28
Ileocolic ulceration: a long-term complication following ileocolic anastomosis. J Pediatr Surg (1988) 1.26
Quantitative RT-PCR assays show Xist RNA levels are low in mouse female adult tissue, embryos and embryoid bodies. Development (1994) 1.25
Involvement of IsK-associated K+ channel in heart rate control of repolarization in a murine engineered model of Jervell and Lange-Nielsen syndrome. Circ Res (1998) 1.25
Neonatal tumours: a thirty-year population-based study. Med Pediatr Oncol (1994) 1.24
Detection of fast neuronal signals in the motor cortex from functional near infrared spectroscopy measurements using independent component analysis. Med Biol Eng Comput (2004) 1.23
Micturition symptoms and unstable bladder activity in girls with primary vesicoureteric reflux. Br J Urol (1982) 1.18
Increased resistance developing in Holter valves. Lancet (1967) 1.18
Ultrasound examinations in pregnancy and childhood cancer. Lancet (1984) 1.17
Caring for survivors of childhood cancers: the size of the problem. Eur J Cancer (2006) 1.15
Copper metabolism in mottled mouse mutants: distribution of 64Cu in brindled (Mobr) mice. Biochem J (1979) 1.15
Orbital tuberculosis in childhood. Br J Ophthalmol (1982) 1.14
A geostatistical approach to the analysis of pattern in rare disease. J Public Health Med (1992) 1.13
Sodium bicarbonate prophylaxis of sickle cell crisis. Pediatrics (1974) 1.13
Genetic polymorphism of lactate dehydrogenase isoenzymes in the carp (Cyprinus carpio) apparently due to a "null allele". Biochem Genet (1973) 1.12
Restriction site mapping of adenovirus type 8 genome types. Res Virol (1991) 1.12
X-rays in pregnancy and the risk of childhood cancer. Lancet (1985) 1.11
Thrombectomy for renal venous thrombosis in infant of diabetic mother. Br Med J (1970) 1.10
[Chromosome aberrations in human lymphocytes in cases of chronic arsenic poisoning]. Dtsch Med Wochenschr (1970) 1.10
[On the topic: longitudinal courses of human palmar ridges]. Humangenetik (1964) 1.10
Study of local cerebral hemodynamics by frequency-domain near-infrared spectroscopy and correlation with simultaneously acquired functional magnetic resonance imaging. Opt Express (2001) 1.09
The Inter-Regional Epidemiological Study of Childhood Cancer (IRESCC): case control study of children with bone and soft tissue sarcomas. Br J Cancer (1988) 1.09
DDK egg-foreign sperm incompatibility in mice is not between the pronuclei. J Reprod Fertil (1986) 1.09
The Inter-Regional, Epidemiological Study of Childhood Cancer (IRESCC): case-control study in children with germ cell tumours. Carcinogenesis (1986) 1.08
Unilateral proptosis. Arch Dis Child (1981) 1.08
Giant cell pneumonia complicating acute lymphoblastic leukemia in remission. Ann Radiol (Paris) (1977) 1.07
Management of leukaemic infiltration of the testis. Arch Dis Child (1980) 1.07
Cisapride reduces neonatal postoperative ileus: randomised placebo controlled trial. Arch Dis Child Fetal Neonatal Ed (1997) 1.07
The role of Epstein-Barr virus in Hodgkin's disease from different geographical areas. Arch Dis Child (1996) 1.06
Thanatophoric dwarfism. J Med Genet (1973) 1.06
An outbreak of multiple-drug-resistant Salmonella enteritis from raw milk. JAMA (1985) 1.06
The Birmingham twin survey. Proc R Soc Med (1968) 1.05
Familiarity, objectivity--and misconduct. Counterstatement to Shaw DM. The Swiss Report on homoeopathy: a case study of research misconduct. Swiss Med Wkly. 2012;142:w13594. Swiss Med Wkly (2013) 1.05
The Inter-Regional Epidemiological Study of Childhood Cancer (IRESCO). Study design, control selection and data collection. Br J Cancer (1985) 1.05
Staged orchiopexy--a new technique. J Pediatr Surg (1975) 1.04
A genetic defect of the C1q subcomponent of complement associated with childhood (immune complex) nephritis. N Engl J Med (1980) 1.04
Childhood cancer and parental use of tobacco: findings from the inter-regional epidemiological study of childhood cancer (IRESCC). Br J Cancer (2001) 1.03
[The mechanism of diploidization in vertebrate evolution: coexistence of tetrasomic and disomic gene loci for the isocitrate dehydrogenases in trout (salmo irideus)]. Humangenetik (1970) 1.03
The Inter-Regional Epidemiological Study of Childhood Cancer (IRESCC): past medical history in children with cancer. J Epidemiol Community Health (1988) 1.02
Studies on the function of H-Y antigen: dissociation and reorganization experiments on rat gonadal tissue. Cytogenet Cell Genet (1978) 1.02
Double outlet right ventricle. Study of 27 cases. Br Heart J (1976) 1.02
Sacrococcygeal teratomas: the UK Children's Cancer Study Group's experience. I. Neonatal. Pediatr Surg Int (2002) 1.02
Radiosensitivity in ataxia-telangiectasia. Br J Radiol (1975) 1.01
Low glutathione peroxidase activity in Gpx1 knockout mice protects jejunum crypts from gamma-irradiation damage. Am J Physiol Gastrointest Liver Physiol (2000) 1.01
Mouse embryos with paternal duplication of an imprinted chromosome 7 region die at midgestation and lack placental spongiotrophoblast. Development (1996) 1.00
Neuroblastomas with chromosome 11q loss and single copy MYCN comprise a biologically distinct group of tumours with adverse prognosis. Br J Cancer (2001) 1.00
Neurofibromatosis with leukaemia. Br Med J (1971) 1.00
Foamy myocardial transformation of infancy: an inherited disease. J Clin Pathol (1987) 1.00
Delta-beta-thalassaemia in a Chinese family. Br J Haematol (1972) 1.00
Coagulation fibrinolysis in sickle-cell disease. J Clin Pathol (1974) 0.99
Duplication of an Xp segment that includes the ZFX locus causes sex inversion in man. Hum Genet (1989) 0.99
Copper metabolism in mottled mouse mutants. Defective placental transfer of 64Cu to foetal brindled (Mobr) mice. Biochem J (1980) 0.99
Insulinoma in childhood. Arch Dis Child (1969) 0.99
Association between hepatoblastoma and polyposis coli. Arch Dis Child (1983) 0.98