Published in Cancer Genet Cytogenet on November 01, 1989
Genital porokeratosis of Mibelli. Genitourin Med (1995) 0.96
Familial craniosynostosis, anal anomalies, and porokeratosis: CAP syndrome. J Med Genet (1998) 0.91
Efficient direct chromosome analyses and enzyme determinations from chorionic villi samples in the first trimester of pregnancy. Hum Genet (1983) 2.93
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223. Hum Genet (1980) 1.87
The 11q;22q translocation: a European collaborative analysis of 43 cases. Hum Genet (1980) 1.82
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal. Nat Genet (1994) 1.78
In vitro study of the DNA replication patterns of somatic chromosomes of Drosophila melanogaster. Exp Cell Res (1966) 1.68
Presumptive x-autosome translocation in a cow: preferential inactivation of the normal x chromosome. Nature (1968) 1.65
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome. Proc Natl Acad Sci U S A (1989) 1.43
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families. Hum Genet (1983) 1.40
Cytogenetics of multiple endocrine neoplasia syndromes. I. Two different, unique clonal chromosome changes in a medullary thyroid carcinoma and in a C-cell thyroid hyperplasia. Cancer Genet Cytogenet (1992) 1.39
Multiple clonal chromosome abnormalities in a superficial basal cell epithelioma. Cancer Genet Cytogenet (1989) 1.38
Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's Syndrome. Hum Genet (1982) 1.28
Women heterozygous for deficiency of the (p21 leads to pter) region of the X chromosome are fertile. Hum Genet (1977) 1.24
A new chromosome instability disorder. Clin Genet (1986) 1.23
Homozygous and compound heterozygous mutations at the Werner syndrome locus. Hum Mol Genet (1996) 1.19
Activity of steroid sulfatase in fibroblasts with numerical and structural X chromosome aberrations. Hum Genet (1981) 1.18
Y chromosome controls mating behaviour on Anopheles mosquitoes. Nature (1977) 1.17
A deletion map of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis. Genomics (1991) 1.12
Expression, topography, and function of integrin receptors are severely altered in keratinocytes from involved and uninvolved psoriatic skin. J Clin Invest (1992) 1.10
Prevalence and distribution of chromosome abnormalities in a sample of first trimester internal abortions. Hum Reprod (1987) 1.02
Evidence for an ancestral alphoid domain on the long arm of human chromosome 2. Hum Genet (1992) 1.01
Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms. Ann Genet (1971) 1.00
Higher plasma catecholamine and metabolite levels in the early phase of nonsegmental vitiligo. Pigment Cell Res (2000) 0.98
A gene controlling H-Y antigen on the X chromosome. Tentative assignment by deletion mapping to Xp223. Hum Genet (1980) 0.98
15/15 translocation in Prader-Willi syndrome. J Med Genet (1977) 0.97
Cytogenetical and clinical investigations in four subjects with anomalies of sexual development. Science (1967) 0.96
X-linked cataract. Ann Hum Genet (1967) 0.95
Incorporation of tritium-labelled actinomycin in a human cell line. Exp Cell Res (1966) 0.95
Diagnostic application of first trimester trophoblast sampling in 100 pregnancies. Hum Genet (1984) 0.94
Male infertility and 13-14 translocation. Lancet (1973) 0.94
Indirect immunofluorescence of inactive centromeres as indicator of centromeric function. Hum Genet (1986) 0.94
Extra minute chromosome in somatic and germ-line cells of the same person. Lancet (1966) 0.93
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1. Cancer Genet Cytogenet (1991) 0.92
Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to Yq. Hum Genet (1993) 0.91
Cytogenetics of multiple endocrine neoplasia syndrome. II. Chromosome abnormalities in an insulinoma and a glucagonoma from two subjects with MEN1. Cancer Genet Cytogenet (1992) 0.91
Localization of Y chromosome sequences and X chromosomal replication studies in XX males. Hum Genet (1989) 0.91
Sex-reversed XY females with campomelic dysplasia are H-Y negative. Hum Genet (1981) 0.91
48,XXXX-49,XXXXX mosaic: asynchronies among the late-replicating X chromosomes. Cytogenetics (1968) 0.90
False-positive and false-negative findings on chorionic villus sampling. Prenat Diagn (1987) 0.90
Timing of DNA replication of translocated Y chromosome sections in somatic cells of Drosophila melanogaster. Chromosoma (1969) 0.90
Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, Mckusick) is at Xq28, distal to the G6PD locus. Hum Genet (1982) 0.88
The gene for human peptidase A is on band 18q23 and shows triplex and uniplex dosage effect. Hum Genet (1978) 0.88
Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment. Hum Genet (1983) 0.88
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 cases. Hum Genet (1982) 0.88
High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequency. Hum Genet (1982) 0.87
Specific instability of the paracentric region of chromosome number 9 in a normal woman and her mongoloid son. Ann Genet (1971) 0.86
Homozygotes for the autosomal dominant neoplasia syndrome (MEN1). Am J Hum Genet (1993) 0.85
Non-fluorescent Y chromosome in a 45,X-46,XY mosaic. Ann Genet (1972) 0.85
BSu restriction of DNA from cases exhibiting sex-chromosome abnormalities. Cytogenet Cell Genet (1978) 0.85
Age of onset in vitiligo: relationship with HLA supratypes. Clin Genet (1991) 0.85
Clinical experience on the treatment of alopecia areata with squaric acid dibutyl ester. Dermatologica (1983) 0.85
Clonal structural chromosomal rearrangements in lymphocytes of four patients with Werner's syndrome. Ann Genet (1990) 0.84
First trimester fetal diagnosis of genetic disorders: clinical evaluation of 250 cases. J Med Genet (1985) 0.84
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome. Am J Hum Genet (1994) 0.83
Xp duplications and sex reversal. Philos Trans R Soc Lond B Biol Sci (1995) 0.83
A novel mechanism for the origin of supernumerary marker chromosomes. Hum Genet (1996) 0.83
Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis. Hum Genet (1987) 0.83
Karyotyping clonal evolution in a cystic adenoma of the ovary. Lancet (1968) 0.83
Timing of sex chromosome replication in somatic and germ-line cells of the mouse and the rat. Cytogenetics (1967) 0.83
XO and male phenotype. Am J Dis Child (1974) 0.82
Additional G-like chromosome in a malformed boy. J Med Genet (1971) 0.82
X chromosomes attached by their long arm: replication autonomy of the short arm adjacent to the inactive centromere. Ann Genet (1977) 0.81
Audiologic disturbances in vitiligo. J Am Acad Dermatol (1989) 0.81
Mucopolysaccharidoses; autoradiographic study of sulphate-35S uptake by cultured fibroblasts. Ann Hum Genet (1968) 0.81
Turner syndrome patients are H-Y positive. Hum Genet (1980) 0.81
Patterns of hair regrowth in alopecia areata. Dermatologica (1988) 0.81
A ZFY-negative 46,XX true hermaphrodite is positive for the Y pseudoautosomal boundary. Hum Genet (1990) 0.81
Nuclear projections and latent centromeres in primary cultures and established cell lines. Prog Clin Biol Res (1978) 0.80
Chromosome abnormalities in tuberous sclerosis. Hum Genet (1988) 0.80
The XY bivalent in human male meiosis. Ann Hum Genet (1966) 0.80
A homozygote for a serum albumin variant of the fast type. Hum Genet (1979) 0.80
Autoimmunity in vitiligo: relationship with HLA, Gm and Km polymorphisms. Autoimmunity (1992) 0.80
Letter: Nuclear projections in tumour cells. Lancet (1974) 0.80
Does confined placental mosaicism affect the fetus? Hum Reprod (1992) 0.79
Risk for recombinants in pericentric inversions of the (p11 leads to q21) region of chromosome 18. Hum Genet (1977) 0.79
Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative study. Hum Genet (1982) 0.79
A 45,X male with a Yp/18 translocation. Hum Genet (1986) 0.79
A homozygote for a serum albumin variant of the slow type. Humangenetik (1975) 0.78
Structural abnormalities of chromosome 18. I. A case of 18q-, with autopsy findings. Ann Genet (1971) 0.78
Human leukocyte antigen region involvement in the genetic predisposition to alopecia areata. Dermatologica (1987) 0.78
Analysis of complex Y chromosome aberrations using a single DNA probe (Y-367). Cytogenet Cell Genet (1989) 0.77
Transposition of 9q34 and 22 (q11toqter) regions has a specific role in chronic myelocytic leukemia. Hum Genet (1979) 0.77
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection. Ann Genet (1991) 0.77
Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18. Ann Genet (1972) 0.77
Chromosomal aberrations in lymphocyte and fibroblast cultures of patients with the sporadic type of Kaposi sarcoma. Hum Genet (1986) 0.77
Presence of H-Y antigen in female patients with sex-chromosome mosaics and absence of testicular tissue. Am J Med Genet (1983) 0.77
Alopecia areata and topical sensitizers: allergic response is necessary but irritation is not. Br J Dermatol (1991) 0.77
Altered cellular response to UV irradiation in a patient affected by premature ageing. Hum Genet (1986) 0.77
Correlation between testicular tissue and H-Y phenotype in intersex patients. Clin Genet (1983) 0.77
Y-dependent polypeptides identified by two-dimensional gel electrophoresis of monozygotic X0 and XY fibroblasts. Hum Genet (1984) 0.77
Possible localization of the genes for the Kidd blood group on an autosome involved in a reciprocal translocation. Nature (1966) 0.76
Karotype, DNA replication and origin of sex chromosomes in Anopheles atroparvus. Chromosoma (1976) 0.76
Some aspects of intracellular symbiosis during embryo development of Mastotermes darwiniensis (Isoptera: Mastotermitidae). Parassitologia (1998) 0.76
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia. J Med Genet (1987) 0.75
A clonal t(9;12)(q32;q21) in cultured fibroblasts from a case of Bowen's disease. Cancer Genet Cytogenet (1989) 0.75
Extravillus dividing fetal cells at CVS: evidence of their erythroblastic origin. J Med Genet (1992) 0.75
Vitiligo and topical allergens. Dermatologica (1989) 0.75
Diphenylcyclopropenone: An important agent known to cause depigmentation. Dermatology (1999) 0.75