Published in Tsitol Genet on September 24, 1996
Unexplained autism is frequently associated with low-level mosaic aneuploidy. J Med Genet (2007) 1.29
Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB). Chromosome Res (2006) 1.18
Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric diseases. Brain Dev (2001) 1.14
Molecular cytogenetics and cytogenomics of brain diseases. Curr Genomics (2008) 1.12
High resolution multicolor fluorescence in situ hybridization using cyanine and fluorescein dyes: rapid chromosome identification by directly fluorescently labeled alphoid DNA probes. Hum Genet (1996) 1.05
Somatic genome variations in health and disease. Curr Genomics (2010) 1.04
Somatic cell genomics of brain disorders: a new opportunity to clarify genetic-environmental interactions. Cytogenet Genome Res (2013) 0.88
Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probes. Prenat Diagn (1995) 0.86
Breast cancer immunohistochemical features in young women with BRCA 1/2 mutations. Exp Oncol (2009) 0.86
Ontogenetic variation of the human genome. Curr Genomics (2010) 0.86
18p- syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence. Hum Genet (1986) 0.86
Trisomy 21 mosaicism: we may all have a touch of Down syndrome. Cytogenet Genome Res (2013) 0.86
Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia. Cytogenet Genome Res (2008) 0.85
[Variations of heterochromatic chromosomal regions and chromosome abnormalities in children with autism: identification of genetic markers in autistic spectrum disorders]. Zh Nevrol Psikhiatr Im S S Korsakova (2006) 0.80
Analysis of alphoid DNA variation and kinetochore size in human chromosome 21: evidence against pathological significance of alphoid satellite DNA diminutions. Tsitol Genet (1999) 0.79
Rapid chromosomal analysis of germ-line cells by FISH: an investigation of an infertile male with large-headed spermatozoa. Mol Hum Reprod (1996) 0.79
[The most frequent chromosomal abnormalities in karyotypes of patients with reproductive problems]. Tsitol Genet (2007) 0.79
[Epigenetic study of Rett's syndrome as an adequate model for autistic disorders]. Zh Nevrol Psikhiatr Im S S Korsakova (2005) 0.79
[Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients]. Zh Nevrol Psikhiatr Im S S Korsakova (2002) 0.78
[Analysis of germ cell populations in ejaculate of men infected with herpes simplex virus]. Ontogenez (2008) 0.78
[Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations]. Zh Nevrol Psikhiatr Im S S Korsakova (2013) 0.78
Clinical, neurophysiological and immunological correlations in classical Rett syndrome. Brain Dev (2001) 0.78
[The use of molecular cytogenetic and cytogenetic techniques for the diagnosis of Prader-Willi and Angelman syndrome]. Zh Nevrol Psikhiatr Im S S Korsakova (2014) 0.78
Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-. Tsitol Genet (2002) 0.77
[Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)]. Zh Nevrol Psikhiatr Im S S Korsakova (2013) 0.77
[Dynamics of changes in anomalous human cells during prolonged cultivation in the stationary phase. Trisomy 7 cells]. Biull Eksp Biol Med (1977) 0.77
[Cytogenetic, molecular cytogenetic, clinical and genealogical study of mothers of children with autism: a search for family genetic markers of autistic disorders]. Zh Nevrol Psikhiatr Im S S Korsakova (2009) 0.76
Double color in situ hybridization of alpha-satellite chromosome 13, 21 specific cosmid clones for a rapid screening of their specificity. Tsitol Genet (1998) 0.76
Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome. Brain Dev (2001) 0.76
[Molecular cytogenetic pre- and postnatal diagnosis of chromosomal abnormalities]. Vestn Ross Akad Med Nauk (1999) 0.76
[Chromosomal mosaicism in spontaneous abortions: analysis of 650 cases]. Genetika (2010) 0.76
[Diagnosis of numerical chromosomal aberrations in the cells of spontaneous abortions by multicolor fluorescence in situ hybridization (MFISH)]. Klin Lab Diagn (2005) 0.76
[Molecular cytogenetic research on the polymorphism of segments of the constitutive heterochromatin in human chromosomes]. Genetika (1988) 0.76
[Chromosome abnormalities in schizophrenia]. Zh Nevrol Psikhiatr Im S S Korsakova (2006) 0.76
[Unusual cases of the inheritance of Down's syndrome]. Tsitol Genet (1988) 0.76
[Current methods of molecular cytogenetics in pre- and postnatal diagnosis of chromosome aberrations]. Klin Lab Diagn (2000) 0.76
Fluorescence intensity profiles of in situ hybridization signals depict genome architecture within human interphase nuclei. Tsitol Genet (2009) 0.76
[X chromosome inactivation pattern in elderly women over 70 years of age]. Tsitol Genet (2005) 0.76
[Molecular cytogenetic methods for studying interphase chromosomes in human brain cells]. Genetika (2010) 0.75
[Unusual case of 18p- syndrome: diagnosis using a cloned DNA fragment]. Tsitol Genet (1986) 0.75
[Original molecular cytogenetic approach to determining spontaneous chromosomal mutations in the interphase cells to evaluate the mutagenic activity of environmental factors]. Gig Sanit (2011) 0.75
[Replication of chromosomal DNA in Chinese hamster cells, cultivated at different temperatures]. Tsitologiia (1977) 0.75
[Optimization of the conditions for the in situ hybridization of cloned DNA sequences and for the differential staining of human chromosomes]. Biull Eksp Biol Med (1984) 0.75
[Discovery of a new family of human alpha-satellite DNA]. Dokl Akad Nauk (1992) 0.75
[Molecular cytogenetic study of Robertsonian translocation 13;14 and Down syndrome in a 3-year-old infant]. Tsitol Genet (2005) 0.75
[A review of the data from cytogenetic and molecular cytogenetic research on human supernumerary minichromosomes]. Tsitol Genet (1995) 0.75
[Cloned fragment of human alphoid DNA--a molecular marker of the pericentromeric region of chromosome 18]. Genetika (1986) 0.75
[Cytogenetic and molecular genetic diagnostics of Rett syndrome in children]. Zh Nevrol Psikhiatr Im S S Korsakova (1998) 0.75
[Characteristics of DNA replication in the long-term culture of human cells at the stationary phase]. Tsitologiia (1987) 0.75
[Genomic instability in the brain: etiology, pathogenesis and new biological markers of psychiatric disorders]. Vestn Ross Akad Med Nauk (2012) 0.75
[Nervous and mental diseases in boys and mutations in MECP2 gene]. Zh Nevrol Psikhiatr Im S S Korsakova (2004) 0.75
[Rate of DNA replication and size of replicons in human diploid cells]. Mol Biol (Mosk) (1979) 0.75
[Molecular genetic polymorphism of the genes of neurotransmitter systems in schizophrenics with early manifestation of the disease]. Zh Nevrol Psikhiatr Im S S Korsakova (2001) 0.75
[A case of deletion of the short arm of the chromosome 21 (21p-) (christchurch chromosome) discovered prenatally:clinical and cytogenetic data]. Tsitol Genet (2004) 0.75
[The search for a mutation in the gene coding the beta-amyloid protein precursor gene in patients with Alzheimer-type dementias]. Zh Nevrol Psikhiatr Im S S Korsakova (1996) 0.75
[Use of a cloned alphoid repetitive sequence of human DNA in studying the polymorphism of heterochromatin regions of chromosomes]. Genetika (1988) 0.75
[Chromosomal anomalies in children with undifferentiated forms of metal retardation based on molecular cytogenetic research data]. Tsitol Genet (1994) 0.75
[Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization]. Genetika (1998) 0.75
[Chromosome organization of human alphoid DNA]. Dokl Akad Nauk SSSR (1986) 0.75
Species specific variant of human centromeric DNA repeats: localization on chromosome 18 and recent amplification in human ancestral line. Mol Gen Mikrobiol Virusol (1989) 0.75
[Structural analysis of the Alu-containing DNA fragment with disperse distribution in human chromosomes]. Genetika (1984) 0.75
[Quantitative analysis of fluorescence in situ hybridization (FISH) signals for molecular cytogenetic diagnosis]. Klin Lab Diagn (2005) 0.75
[Molecular-cytogenetic diagnosis of hereditary diseases associated with diverse anomalies of X chromosome]. Pediatriia (1989) 0.75
[Serotonin type 2a (5-HTR2A) receptor gene polymorphism and personality traits in patients with endogenous psychoses]. Genetika (2001) 0.75
[Cloned fragment of human repetitive DNA specific for the centromere heterochromatin of chromosome 3]. Mol Gen Mikrobiol Virusol (1986) 0.75
[Correlation of polymorphism of heterochromatin segments with hybridization on chromosome preparations of various cloned repeated human DNA sequences]. Genetika (1989) 0.75
[Development of an original computer program FISHMet: use for molecular cytogenetic diagnosis and genome mapping by fluorescent in situ hybridization (FISH)]. Klin Lab Diagn (2000) 0.75
[Instability of chromosomes in human nerve cells (normal and with neuromental diseases)]. Genetika (2010) 0.75
[Interindividual hyperpolymorphism of autosomal satellites III of human DNA]. Genetika (1990) 0.75
[DNA replication in cultured amniotic fluid cells]. Biull Eksp Biol Med (1981) 0.75
[Serotonin receptor gene allele polymorphism (5HTR2A) and clinical pathogenetic characteristics in patients with schizophrenia and schizophrenia spectrum disorders]. Zh Nevrol Psikhiatr Im S S Korsakova (2000) 0.75
[Molecular genetics of the human brain]. Vestn Ross Akad Med Nauk (1992) 0.75
[A method of analyzing the chromosome localization of repetitive nucleotide sequences by using hybridization in situ]. Genetika (1988) 0.75
[DNA replication in a primary culture of human hepatocytes]. Dokl Akad Nauk SSSR (1976) 0.75
[A familial case of mental retardation syndrome linked to fragile X chromosome]. Zh Nevrol Psikhiatr Im S S Korsakova (1998) 0.75
[Rate of DNA synthesis and the size of replication units in cell culture of Drosophila melanogaster]. Mol Biol (Mosk) (1979) 0.75
[A cytogenetic study of the human chorion for the purpose of the prenatal diagnosis of hereditary diseases]. Tsitologiia (1990) 0.75
[Method of diagnosing aneuploidies using in situ hybridization: analysis of interphase nuclei]. Biull Eksp Biol Med (1991) 0.75
[Contemporary views on Rett's syndrome: clinical, cytogenetic and molecular studies]. Zh Nevrol Psikhiatr Im S S Korsakova (1999) 0.75
[Quantitative analysis of chromosomal localization of two human cloned satellite DNA III sequences by in situ hybridization]. Genetika (1989) 0.75
[Multidisciplinary approach to the study of a family with many children including several schizophrenics]. Zh Nevropatol Psikhiatr Im S S Korsakova (1992) 0.75
[The use of modern diagnostic and preventive technologies in children with hereditary and congenital intellectual developmental disorders]. Vestn Ross Akad Med Nauk (2006) 0.75
[Clones sequences of satellite DNA III specific for the centromere heterochromatin of human chromosome 9]. Mol Gen Mikrobiol Virusol (1986) 0.75
[Mental retardation syndrome due to fragile X chromosome: diagnostic and genetic problems]. Zh Nevrol Psikhiatr Im S S Korsakova (1998) 0.75