Published in Ann Genet on December 01, 1975
Further dicentric X isochromosomes and deletions, and a new structure i(X)(pter to q2102 to pter). J Med Genet (1979) 0.96
Two cases of ring chromosome 11. J Med Genet (1983) 0.84
Cytogenetic and clinical studies in gonadal dysgenesis with 46,X,Xt(qter leads to p221::p223 leads to qter) karyotype: review and phenotype/karyotype correlations. J Med Genet (1980) 0.81
Distribution of break points in human structural rearrangements. Am J Hum Genet (1983) 0.81
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
Risk factors for anastomotic leakage after resection of rectal cancer. Br J Surg (1998) 3.45
[A new technic of analysis of the human karyotype]. C R Acad Sci Hebd Seances Acad Sci D (1971) 2.62
Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Mol Psychiatry (2008) 2.07
[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
A multicentre, randomised phase II study of weekly or 3-weekly docetaxel in patients with metastatic breast cancer. Ann Oncol (2004) 1.85
NSD3, a new SET domain-containing gene, maps to 8p12 and is amplified in human breast cancer cell lines. Genomics (2001) 1.85
Intersphincteric resection with excision of internal anal sphincter for conservative treatment of very low rectal cancer. Dis Colon Rectum (1999) 1.83
Chromosomal evolution in primates: tentative phylogeny from Microcebus murinus (Prosimian) to man. Hum Genet (1979) 1.75
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. Am J Hum Genet (2000) 1.68
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
A strategy for optimizing the monodispersity of fusion proteins: application to purification of recombinant HPV E6 oncoprotein. Protein Eng (2001) 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
[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
[Acupuncture worth trying in severe tinnitus]. Lakartidningen (1998) 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 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
[Children arthropod bites protective measures: insecticides and repellents]. Arch Pediatr (2007) 1.39
RFLP identified by the anonymous DNA segment OL VII E10 at 18q21.3 (HGM no. D18S8). Nucleic Acids Res (1987) 1.38
High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia. Mutat Res (1980) 1.38
Constitutional balanced translocations in patients with solid tumors. Cancer Genet Cytogenet (1992) 1.38
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
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
Loop ileostomy versus loop colostomy for defunctioning low anastomoses during rectal cancer surgery. World J Surg (2001) 1.30
Formation of soluble inclusion bodies by hpv e6 oncoprotein fused to maltose-binding protein. Protein Expr Purif (2001) 1.29
Characterization of a selective and potent antagonist of human P2X(7) receptors, AZ11645373. Br J Pharmacol (2006) 1.29
In-vitro activity of erythromycin, roxithromycin and CP 62993 against common paediatric pathogens. J Antimicrob Chemother (1987) 1.26
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
Malignant extraovarian endometriosis: a review. Eur J Surg Oncol (2005) 1.23
[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
Control of myogenesis in the mouse myogenic C2 cell line by medium composition and by insulin: characterization of permissive and inducible C2 myoblasts. Differentiation (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
Liver resection of colorectal metastases in elderly patients. Br J Surg (2010) 1.21
Genes occupy a fixed and symmetrical position on sister chromatids. Cell (1991) 1.20
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
The oncological safety of laparoscopic total mesorectal excision with sphincter preservation for rectal carcinoma. Surg Endosc (2005) 1.17
Second-generation three-dimensional reconstruction for rotational three-dimensional angiography. Acad Radiol (1998) 1.17
[Four new cases of X-autosome translocation in man (author's transl)]. Humangenetik (1975) 1.17
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
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
DNA hypomethylation in breast cancer: an independent parameter of tumor progression? Cancer Genet Cytogenet (1997) 1.11
Proto-oncogene amplification and homogeneously staining regions in human breast carcinomas. Genes Chromosomes Cancer (1990) 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
Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE. Transl Psychiatry (2012) 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
Loss of alleles on chromosome 18 and on the short arm of chromosome 17 in polyploid colorectal carcinomas. Int J Cancer (1988) 1.08
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
[Genetic and clinical study of a family of 7 children in which 3 persons have "crying cat syndrome"]. Ann Genet (1966) 1.07
Adult human masseter muscle fibers express myosin isozymes characteristic of development. Muscle Nerve (1988) 1.06
Comparison of RBG-banded karyotypes of cattle, sheep, and goats. Cytogenet Cell Genet (1991) 1.06
A multicenter cohort study to compare quality of life in breast cancer patients according to sentinel lymph node biopsy or axillary lymph node dissection. Ann Oncol (2009) 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
Exploring multifunctional agriculture. A review of conceptual approaches and prospects for an integrative transitional framework. J Environ Manage (2009) 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
Hyaluronan and healing of tympanic membrane perforations. An experimental study. Acta Otolaryngol Suppl (1987) 1.04
[Partial monosomy 20q: a new syndrome. Regional assignment of the adenosine deaminase (ADA) locus on 20q132 (author's transl)]. Ann Genet (1981) 1.03
[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
Correlates of intake of folic acid-containing supplements among pregnant women. Am J Obstet Gynecol (2006) 1.02
Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder. Mol Psychiatry (2004) 1.01
Variations of chromosome radiation sensitivity in fetal and adult mice during gestation. Mutat Res (1991) 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
Regional assignment of the ADA locus on 20q13.2 leads to qter by gene dosage studies. Cytogenet Cell Genet (1980) 1.01
Z-DNA immunoreactivity in fixed metaphase chromosomes of primates. Proc Natl Acad Sci U S A (1983) 1.01
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
Novel P2X7 receptor antagonists. Bioorg Med Chem Lett (2003) 1.00
Common methylation characteristics of sex chromosomes in somatic and germ cells from mouse, lemur and human. Chromosome Res (2000) 1.00
Hepatic undifferentiated embryonal sarcoma: malignant evolution of mesenchymal hamartoma? Study of one case with immunohistochemical and flow cytometric emphasis. J Hepatol (2001) 1.00
[Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)]. Ann Genet (1976) 1.00
Identification of a human guanine nucleotide-releasing factor (H-GRF55) specific for Ras proteins. Oncogene (1993) 0.99
Fine mapping of human HOX gene clusters. Cytogenet Cell Genet (1996) 0.99