Published in J Med Genet on December 01, 1986
Review and hypotheses: somatic mosaicism: observations related to clinical genetics. Am J Hum Genet (1988) 3.05
Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests. Proc Natl Acad Sci U S A (1990) 2.50
Germ-line mosaicism in tuberous sclerosis: how common? Am J Hum Genet (1999) 1.12
Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening. J Med Genet (1989) 1.02
Mosaicism with a normal cell line and an autosomal structural rearrangement. J Med Genet (1994) 0.92
Germinal mosaicism and risk calculation in X-linked diseases. Am J Hum Genet (1992) 0.92
Parental somatic and germ-line mosaicism for a multiexon deletion with unusual endpoints in a type III collagen (COL3A1) allele produces Ehlers-Danlos syndrome type IV in the heterozygous offspring. Am J Hum Genet (1993) 0.89
Molecular diagnosis of duchenne muscular dystrophy: past, present and future in relation to implementing therapies. Clin Biochem Rev (2011) 0.83
A simple method for calculating risks before DNA analysis. J Med Genet (1988) 0.77
Imperatives for DUCHENNE MD: a Simplified Guide to Comprehensive Care for Duchenne Muscular Dystrophy. PLoS Curr (2015) 0.76
The population genetics of Duchenne muscular dystrophy. J Med Genet (1988) 0.75
Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. Am J Hum Genet (1974) 23.66
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature (1986) 4.13
Mutation in the sex-linked recessive type of muscular dystrophy; a possible sex difference. Ann Hum Genet (1956) 1.71
The analysis of X-linkage. Ann Hum Genet (1971) 1.71
Huntington disease: estimation of heterozygote status using linked genetic markers. Genet Epidemiol (1984) 1.39
The genetic status of mothers of isolated cases of Duchenne muscular dystrophy. J Med Genet (1983) 1.32
The use of flanking markers in prediction for Duchenne muscular dystrophy. Arch Dis Child (1986) 1.19
A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional information. J Med Genet (1986) 0.98
A computer programme to calculate risk in X linked disorders using multiple marker loci. J Med Genet (1986) 0.93
The history of a lethal X-linked mutant. IMA J Math Appl Med Biol (1985) 0.88
Duchenne muscular dystrophy. J Med Genet (1984) 0.88
Old problems in new clothes. Lancet (1985) 0.87
The use of computers. Cytogenet Cell Genet (1982) 8.57
Report of the Committee on Methods of Linkage Analysis and Reporting. Cytogenet Cell Genet (1985) 5.61
Familial predisposition in man. Br Med Bull (1969) 5.15
The incidence of malformations in Birmingham, England, 1950-1959. Teratology (1968) 3.69
Chromosome maps of man and mouse. IV. Ann Hum Genet (1989) 2.25
Protozoa as sources of antigen in 'humidifier fever'. Nature (1976) 2.06
The analysis of X-linkage. Ann Hum Genet (1971) 1.71
An investigation of the difference in measured intelligence between twins and single births. Ann Hum Genet (1970) 1.67
The relation of measured intelligence to birth weight and duration of gestation. Ann Hum Genet (1969) 1.56
The relation of measured intelligence to birth order and maternal age. Ann Hum Genet (1969) 1.52
Three cases of triploidy in man. Cytogenetics (1967) 1.48
The double dialysis method of producing farmer's lung antigens. J Lab Clin Med (1972) 1.45
Unifactorial models are not appropriate for multifactorial disease. BMJ (1999) 1.39
Chromosome maps of man and mouse, III. Genomics (1987) 1.39
De Lange syndrome: report of 20 cases. Can Med Assoc J (1967) 1.31
Patau's syndrome with D 1 duplication-deficenncy derived from a maternal D group pericentric inversion. Ann Hum Genet (1971) 1.31
The composition of massive lesions in coal miners. Thorax (1975) 1.30
Very close linkage between HLA-B and Bf inferred from allelic association. Nature (1977) 1.30
The interpretation of lods in linkage analysis. Cytogenet Cell Genet (1976) 1.26
A quantitative study on the activation of the alternative pathway of complement by mouldy hay dust and thermophilic actinomycetes. Clin Allergy (1976) 1.24
Mouse homologues of human hereditary disease. J Med Genet (1994) 1.22
Obstetric complications and school performance. Br Med J (1967) 1.21
Cross-reacting antibodies to Micropolyspora faeni in Mycoplasma pneumoniae infection. Clin Allergy (1975) 1.21
Macrophage responses to mouldy hay dust, Micropolyspora faeni and zymosan, activators of complement by the alternative pathway. Clin Exp Immunol (1977) 1.21
Lead levels in human placentae from normal and malformed births. J Med Genet (1977) 1.20
Pulmonary responses to particulate materials capable of activating the alternative pathway of complement. Clin Allergy (1976) 1.20
A marker algebra. Clin Genet (1972) 1.17
The blood groups of Icelanders. Ann Hum Genet (1973) 1.12
Microbial and immunological investigations and remedial action after an outbreak of humidifier fever. Br J Ind Med (1980) 1.12
The mutation rate in man. Prog Med Genet (1974) 1.12
DNA polymorphism of the C2 and factor B genes. Detection of a restriction fragment length polymorphism which subdivides haplotypes carrying the C2C and factor B F alleles. Immunogenetics (1985) 1.12
Caution in locating the gene(s) for affective disorder. Psychol Med (1989) 1.11
Coeliac disease and lung disease. Lancet (1971) 1.09
Humidifier fever in an operating theatre. Br Med J (1979) 1.07
Absorption of serum proteins by inorganic dusts. Br J Ind Med (1972) 1.07
Chromosome maps of man and mouse II. Clin Genet (1984) 1.06
Heterocellular hereditary persistence of fetal haemoglobin (heterocellular HPFH) and its interaction with beta thalassaemia. Br J Haematol (1977) 1.05
Antigens in pigeon breeders' disease. Immunology (1970) 1.05
An exclusion map for Von Recklinghausen neurofibromatosis. J Med Genet (1987) 1.05
Grain exposure--symptoms and lung function. Eur J Respir Dis (1983) 1.04
Monozygotic twins of different sex. J Med Genet (1966) 1.04
A comparison of albumin and urea as reference markers in bronchoalveolar lavage fluid from patients with interstitial lung disease. Eur Respir J (1990) 1.02
Short bouts of mechanical loading are as effective as dexamethasone at inducing matrix production by human bone marrow mesenchymal stem cell. Eur Cell Mater (2010) 0.99
Correlation between a DNA restriction fragment length polymorphism and C4A6 protein. Nature (1984) 0.99
A search for linkage in cystic fibrosis. J Med Genet (1976) 0.99
Aetiology and outcomes of adult superior oblique palsies: a modern series. Eye (Lond) (2008) 0.97
Hypersensitivity pneumonitis after exposure to isocyanates. Thorax (1976) 0.97
A meiotic linkage map of the human male. Cytogenet Cell Genet (1978) 0.97
The estimation of risks from the induction of recessive mutations after exposure to ionising radiation. J Med Genet (1986) 0.96
An attempt to map two genes for tuberous sclerosis using novel two-point methods. Ann N Y Acad Sci (1991) 0.93
Amendment effects on soil test phosphorus. J Environ Qual (2005) 0.93
Multiple pregnancy: the value of twins in genetic studies. Proc R Soc Med (1968) 0.92
Chromosome maps of man and mouse. Clin Genet (1981) 0.91
Excretion of pigeon serum proteins in pigeon droppings. Proc Soc Exp Biol Med (1969) 0.91
Centrometric linkage in autosomal trisomies. Ann Hum Genet (1975) 0.90
Ispaghula sensitization in workers manufacturing a bulk laxative. Clin Exp Allergy (1990) 0.90
Centromeric linkage. Birth Defects Orig Artic Ser (1975) 0.89
Serum creatine kinase levels in pubertal, mature, pregnant, and postmenopausal women. J Med Genet (1979) 0.89
Heterogeneity of human C4 gene size. A large intron (6.5 kb) is present in all C4A genes and some C4B genes. Immunogenetics (1987) 0.89
Duchenne muscular dystrophy. J Med Genet (1984) 0.88
Measurement of interleukin-6 in bronchoalveolar lavage fluid by radioimmunoassay: differences between patients with interstitial lung disease and control subjects. Clin Exp Immunol (1991) 0.88
Inhalation challenge in humidifier fever. Clin Allergy (1981) 0.87
The value of twin surveys in the study of malformations. Eur J Obstet Gynecol Reprod Biol (1983) 0.87
Arrhinencephaly associated with a deficiency involving chromosome 18. J Med Genet (1968) 0.87
On the distribution of phenotypes in XXY males and their parents. J Med Genet (1971) 0.87
Old problems in new clothes. Lancet (1985) 0.87
Pseudoimmune precipitation by the isolated byssinosis "antigen". J Immunol (1973) 0.86
Immunology of byssinosis: a study of the reactions between the isolated byssinosis "antigen" and human immunoglobulins. Ann N Y Acad Sci (1974) 0.85
0.6 T MR imaging of the cervical spine: multislice and multiecho techniques. AJNR Am J Neuroradiol (1985) 0.85
Mono-amniotic twins. J Obstet Gynaecol Br Commonw (1968) 0.85
DNA probes in X-linked disease. Lancet (1983) 0.85
Spina bifida trials. Nature (1983) 0.84
Byssinosis. Inhalation challenge with polyphenol. Chest (1984) 0.84
Inhalation challenge and skin testing in farmer's lung. J Allergy Clin Immunol (1981) 0.84
Angiographically undetected ulceration of the carotid bifurcation as a cause of embolic stroke. Radiology (1979) 0.84
Locus for cystic fibrosis. Lancet (1984) 0.83
Immunoregulatory proteins in bronchoalveolar lavage fluid. A comparative analysis of pigeon breeders' disease, sarcoidosis and idiopathic pulmonary fibrosis. Sarcoidosis (1989) 0.83
Access to data on humans. Nature (1996) 0.83
Population genetics of C4 with the use of complementary DNA probes. Philos Trans R Soc Lond B Biol Sci (1984) 0.83
Heterozygote advantage. Arch Dis Child (1977) 0.83
Proceedings: Total lods for linkage analyzed by the New York Blood Center and Birmingham Computer Programs. Cytogenet Cell Genet (1974) 0.83
Immunoglobulin and antibody levels in bronchoalveolar lavage fluid from symptomatic and asymptomatic pigeon breeders. Clin Exp Immunol (1991) 0.82
Sex ratio in phenylketonuria. Lancet (1970) 0.82
Probes in Huntington's chorea. Nature (1986) 0.82
Allergy to inhaled egg material. Clin Allergy (1983) 0.82
The need for care in the use of linkage analysis for genetic diagnosis in small families, with particular reference to uniparental disomy. Am J Hum Genet (1992) 0.81
Genetic markers in trisomies 13 and 18. Ann Hum Genet (1976) 0.81
Early diagnosis of Duchenne's disease. Lancet (1979) 0.81
Humidifier fever. R Soc Health J (1982) 0.80
Skeletal muscle bioenergetics in myotonic dystrophy. J Neurol Sci (1993) 0.80
Amniocentesis in the West Midlands: report on 1000 births. J Med Genet (1980) 0.79
Centromeric linkage. Cytogenet Cell Genet (1975) 0.79
Letter: Gluten and myasthenia gravis. Lancet (1975) 0.79
The isolation of antigens associated with farmer's lung. Clin Exp Immunol (1972) 0.79
The effect of ultrasonic cavitation on protein antigenicity. J Acoust Soc Am (1976) 0.78
Amniocentesis rates in older women. Lancet (1979) 0.77
Data on linkage between the locus determining placental alkaline phosphatase (Pl) and other markers. Ann Hum Genet (1967) 0.77
Doubt about evidence for a schizophrenia gene on chromosome 5. Psychol Med (1991) 0.77
Alprazolam: an antidepressant? Alprazolam, desipramine, and an alprazolam-desipramine combination in the treatment of adult depressed outpatients. J Clin Psychopharmacol (1987) 0.76
Report of the second international workshop on human chromosome 14 mapping 1994. Cytogenet Cell Genet (1995) 0.76