Published in Humangenetik on January 01, 1975
Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus. J Med Genet (1981) 2.10
Analysis of deoxyribonucleic acid replication in human X chromosomes by fluorescence microscopy. Am J Hum Genet (1976) 1.90
Gonadal dysgenesis in a patient with an X;3 translocation: case report and review. J Med Genet (1980) 1.40
X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci. J Med Genet (1979) 1.00
Short stature in a girl with a terminal Xp deletion distal to DXYS15: localisation of a growth gene(s) in the pseudoautosomal region. J Med Genet (1992) 0.97
Inactivation centers in the human X chromosome. Am J Hum Genet (1982) 0.76
Requirement of poly(ADP-ribose) polymerase in recovery from DNA damage in mice and in cells. Proc Natl Acad Sci U S A (1997) 5.24
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. Nat Genet (1997) 3.03
[A new technic of analysis of the human karyotype]. C R Acad Sci Hebd Seances Acad Sci D (1971) 2.62
[Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1]. Exp Cell Res (1976) 2.07
High resolution R- and G-banding on the same preparation. Hum Genet (1981) 1.94
[Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]. C R Acad Sci Hebd Seances Acad Sci D (1973) 1.89
NSD3, a new SET domain-containing gene, maps to 8p12 and is amplified in human breast cancer cell lines. Genomics (2001) 1.85
Chromosomal evolution in primates: tentative phylogeny from Microcebus murinus (Prosimian) to man. Hum Genet (1979) 1.75
A simple method for simultaneous R- or G-banding and fluorescence in situ hybridization of small single-copy genes. Cytogenet Cell Genet (1992) 1.64
Systematic analysis of 95 reciprocal translocations of autosomes. Hum Genet (1978) 1.59
Mapping of single-copy DNA sequences on human chromosomes by in situ hybridization with biotinylated probes: enhancement of detection sensitivity by intensified-fluorescence digital-imaging microscopy. Proc Natl Acad Sci U S A (1989) 1.59
The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications. Am J Hum Genet (1996) 1.53
[Apropos of trisomy 18 - a study of 4 observations]. Ann Genet (1967) 1.53
[Trisomy for the distal part of the short arm of the number 3 chromosome in 3 siblings. First example of chromosomal insertion: INS(7;3)(q 31;p 21 p 26)]. Ann Genet (1972) 1.50
Mutations in OGG1, a gene involved in the repair of oxidative DNA damage, are found in human lung and kidney tumours. Oncogene (1998) 1.49
The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15. Am J Hum Genet (1990) 1.45
Translocation (X;9)(p11;q34) in a girl with incontinentia pigmenti (IP): implications for the regional assignment of the IP locus to Xp11? Ann Genet (1985) 1.42
[The Dr phenotype: a study of threee cases with a ring D chromosome]. Ann Genet (1968) 1.41
[Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)]. Cytogenet Cell Genet (1973) 1.40
Emergence and scattering of multiple neurofibromatosis (NF1)-related sequences during hominoid evolution suggest a process of pericentromeric interchromosomal transposition. Hum Mol Genet (1997) 1.40
RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM no. D18S8). Nucleic Acids Res (1987) 1.38
Constitutional balanced translocations in patients with solid tumors. Cancer Genet Cytogenet (1992) 1.38
High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia. Mutat Res (1980) 1.38
Deficiency of coagulation factors VII and X associated with deletion of a chromosome 13 (q34). Evidence from two cases with 46,XY,t(13;Y)(q11;q34). Hum Genet (1982) 1.37
Sequence of DNA replication in 277 R- and Q-bands of human chromosomes using a BrdU treatment. Chromosoma (1976) 1.36
[The mechanism of chromosome segmentation induced by BUDR (5-bromodeoxyuridine)]. Ann Genet (1974) 1.35
Sensitivity to CPT-11 of xenografted human colorectal cancers as a function of microsatellite instability and p53 status. Br J Cancer (2000) 1.32
Cloning and characterization of the human choroideremia gene. Hum Mol Genet (1994) 1.31
Detection of DNA amplification in 17 primary breast carcinomas with homogeneously staining regions by a modified comparative genomic hybridization technique. Genes Chromosomes Cancer (1994) 1.30
Physical mapping of human loci homologous to the chicken nov proto-oncogene. Oncogene (1992) 1.26
Identification of amplified DNA sequences in breast cancer and their organization within homogeneously staining regions. Genes Chromosomes Cancer (1995) 1.24
SOD2: a new type of tumor-suppressor gene? Int J Cancer (1992) 1.24
[Giemsa-R-banding analysis of the trisomy 9p and report of a new case]. Humangenetik (1973) 1.23
[New system of chromosome banding: the T bands (author's transl)]. Chromosoma (1973) 1.23
Interstitial deletion of chromosome 15: two cases. Hum Genet (1988) 1.22
Selective endoreduplication or branched chromosome? Exp Cell Res (1977) 1.22
[Chromosome 8 : complete trisomy and segmental trisomies]. Ann Genet (1977) 1.22
Genes occupy a fixed and symmetrical position on sister chromatids. Cell (1991) 1.20
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region. Am J Hum Genet (1995) 1.18
Deletion proximal to DXS68 locus (L1 probe site) in a boy with Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal hypoplasia. Hum Genet (1988) 1.18
Establishment and characterisation of a new tumorigenic cell line with a normal karyotype derived from a human breast adenocarcinoma. Br J Cancer (1990) 1.17
[Four new cases of X-autosome translocation in man (author's transl)]. Humangenetik (1975) 1.17
High glycolysis in gliomas despite low hexokinase transcription and activity correlated to chromosome 10 loss. Br J Cancer (1996) 1.17
Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21). Hum Genet (1979) 1.17
The cell cycle of lymphocytes in Fanconi anemia. Hum Genet (1982) 1.16
[Study of progeny of individuals bearing a t(DqDq) translocation]. Ann Genet (1970) 1.15
Increased p53 protein content of colorectal tumours correlates with poor survival. Br J Cancer (1992) 1.13
[Partial trisomy 21 (21q21 - 21q22.2)]. Ann Genet (1976) 1.12
Cytogenetic study of breast cancer: clinicopathologic significance of homogeneously staining regions in 84 patients. Hum Pathol (1992) 1.12
Proto-oncogene amplification and homogeneously staining regions in human breast carcinomas. Genes Chromosomes Cancer (1990) 1.11
DNA hypomethylation in breast cancer: an independent parameter of tumor progression? Cancer Genet Cytogenet (1997) 1.11
Gliomas are driven by glycolysis: putative roles of hexokinase, oxidative phosphorylation and mitochondrial ultrastructure. Anticancer Res (1997) 1.10
Deletion of band 13q21 is compatible with normal phenotype. Hum Genet (1985) 1.09
Loss of alleles on chromosome 18 and on the short arm of chromosome 17 in polyploid colorectal carcinomas. Int J Cancer (1988) 1.08
Cytogenetics of colorectal adenocarcinomas. Cancer Genet Cytogenet (1990) 1.08
[Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21]. Ann Genet (1973) 1.08
Duplication 15q22 to 15qter and its phenotypic expression. Hum Genet (1981) 1.08
Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221. Hum Genet (1984) 1.07
Simultaneous monitoring of P53 protein and DNA content of colorectal adenocarcinomas by flow cytometry. Int J Cancer (1990) 1.07
An unbalanced 4q-21q translocation identified by the R but not by the G and Q chromosome banding techniques. Ann Genet (1973) 1.07
Comparison of RBG-banded karyotypes of cattle, sheep, and goats. Cytogenet Cell Genet (1991) 1.06
Amplification of DNA sequences from chromosome 19q13.1 in human pancreatic cell lines. Genomics (1998) 1.06
Highly recurrent der(1;16)(q10;p10) and other 16q arm alterations in lobular breast cancer. Genes Chromosomes Cancer (1998) 1.06
Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatin. Cytogenet Cell Genet (1993) 1.05
Alterations of DNA methylation patterns in germ cells and Sertoli cells from developing mouse testis. Cytogenet Cell Genet (1999) 1.05
Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1. Hum Mol Genet (1996) 1.04
[Ring 15 chromosome: r(15). Identification by controlled denaturation]. Ann Genet (1972) 1.03
Assignment of human desmin gene to band 2q35 by nonradioactive in situ hybridization. Hum Genet (1989) 1.03
Reconstruction of the ancestral karyotype of eutherian mammals. Chromosome Res (2003) 1.02
Intracellular pH governs the subcellular distribution of hexokinase in a glioma cell line. Biochem J (1996) 1.02
Z-DNA immunoreactivity in fixed metaphase chromosomes of primates. Proc Natl Acad Sci U S A (1983) 1.01
Characterization of SRp46, a novel human SR splicing factor encoded by a PR264/SC35 retropseudogene. Mol Cell Biol (1998) 1.01
Osteosarcoma following retinoblastoma: age at onset and latency period. Ophthalmic Genet (2001) 1.01
Variations of chromosome radiation sensitivity in fetal and adult mice during gestation. Mutat Res (1991) 1.01
c-Ha-ras1 is not deleted in aniridia-Wilms' tumour association. Nature (1983) 1.01
Probable localisation of the Coffin-Lowry locus in Xp22.2-p22.1 by multipoint linkage analysis. Am J Med Genet (1988) 1.01
[Fragile site on chromosome 2 (q11) in a case of familial lymphohistiocytosis]. J Genet Hum (1984) 1.00
Consistent deficiencies of chromosome 18 and of the short arm of chromosome 17 in eleven cases of human large bowel cancer: a possible recessive determinism. Ann Genet (1985) 1.00
Common methylation characteristics of sex chromosomes in somatic and germ cells from mouse, lemur and human. Chromosome Res (2000) 1.00
[Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)]. Ann Genet (1976) 1.00
Fine mapping of human HOX gene clusters. Cytogenet Cell Genet (1996) 0.99
Hypomethylation of classical satellite DNA and chromosome instability in lymphoblastoid cell lines. Hum Genet (1993) 0.99
Identification of a human guanine nucleotide-releasing factor (H-GRF55) specific for Ras proteins. Oncogene (1993) 0.99
Dihydrofolate reductase gene amplification-associated shift of differentiation in methotrexate-adapted HT-29 cells. J Cell Biol (1991) 0.99
Segmentation of human chromosomes induced by 5-ACR (5-azacytidine). Hum Genet (1976) 0.99
[Application of the controlled denaturation method: denaturation of previously stained preparations]. Ann Genet (1972) 0.98
[Mitotic and meiotic analysis of an Y-autosome translocation(author's transl)]. Humangenetik (1975) 0.98
Oncogene amplification in human gliomas: a molecular cytogenetic analysis. Oncogene (1994) 0.97
[The Dr syndrome. Study of a further case (46, XX, 14r)]. Ann Genet (1971) 0.97
The peripheral benzodiazepine receptors: a review. J Neurooncol (2000) 0.97
[A second example of telomeric fusion 2 X chromosomes]. Ann Genet (1975) 0.97
Chromosomal assignment of two human B-raf(Rmil) proto-oncogene loci: B-raf-1 encoding the p94Braf/Rmil and B-raf-2, a processed pseudogene. Oncogene (1992) 0.97
Predominance of normal karyotype in colorectal tumors from hereditary non-polyposis colorectal cancer patients. Genes Chromosomes Cancer (1995) 0.97
[Effect of the ionic medium on controlled heat denaturation of human chromosomes]. Ann Genet (1972) 0.96
Sex chromosome rearrangements in Polyphaga beetles. Sex Dev (2009) 0.96
Distinct chromosomal alterations associated with TP53 status of LoVo cells under PALA selective pressure: a parallel with cytogenetic pathways of colorectal cancers. Oncogene (1999) 0.96
Clinical and experimental progression of a new model of human prostate cancer and therapeutic approach. Am J Pathol (2001) 0.95
Recurrent cytogenetic alterations of prostate carcinoma and amplification of c-myc or epidermal growth factor receptor in subclones of immortalized PNT1 human prostate epithelial cell line. Int J Cancer (1995) 0.95
Genetic evolution of breast cancers. III: Age-dependent variations in the correlations between biological indicators of prognosis. Breast Cancer Res Treat (1995) 0.95
Characterization of chromosome changes in two human prostatic carcinoma cell lines (PC-3 and DU145) using chromosome painting and comparative genomic hybridization. Cancer Genet Cytogenet (1997) 0.95