Published in Zh Nevrol Psikhiatr Im S S Korsakova on January 01, 1998
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
Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders. Neurosci Behav Physiol (2007) 0.93
Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys). Brain Dev (2001) 0.88
Somatic cell genomics of brain disorders: a new opportunity to clarify genetic-environmental interactions. Cytogenet Genome Res (2013) 0.88
Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome. Tsitol Genet (2006) 0.87
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
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
Ontogenetic variation of the human genome. Curr Genomics (2010) 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
Cytogenetic, molecular-cytogenetic, and clinical-genealogical studies of the mothers of children with autism: a search for familial genetic markers for autistic disorders. Neurosci Behav Physiol (2010) 0.84
Cytogenetic and molecular-cytogenetic investigation of Rett syndrome: analysis of 31 cases. Neuroreport (1996) 0.82
[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
Chimerism and multiple numerical chromosome imbalances in a spontaneously aborted fetus. Tsitol Genet (2007) 0.80
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
[Epigenetic study of Rett's syndrome as an adequate model for autistic disorders]. Zh Nevrol Psikhiatr Im S S Korsakova (2005) 0.79
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
[Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients]. Zh Nevrol Psikhiatr Im S S Korsakova (2002) 0.78
Clinical, neurophysiological and immunological correlations in classical Rett syndrome. Brain Dev (2001) 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
[Analysis of germ cell populations in ejaculate of men infected with herpes simplex virus]. Ontogenez (2008) 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
16q subtelomeric deletion in proband with congenital malformations and mental retardation. Tsitol Genet (2001) 0.77
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
Rapid identification of marker chromosomes by in situ hybridization under different stringency conditions. Anal Cell Pathol (1994) 0.77
[Molecular cytogenetic research on the polymorphism of segments of the constitutive heterochromatin in human chromosomes]. Genetika (1988) 0.76
[Molecular cytogenetic pre- and postnatal diagnosis of chromosomal abnormalities]. Vestn Ross Akad Med Nauk (1999) 0.76
Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome. Brain Dev (2001) 0.76
Pericentric inversion inv(7)(p11q21.1): report on two cases and genotype-phenotype correlations. Tsitol Genet (2006) 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
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
[X chromosome inactivation pattern in elderly women over 70 years of age]. Tsitol Genet (2005) 0.76
[Chromosomal mosaicism in spontaneous abortions: analysis of 650 cases]. Genetika (2010) 0.76
[Current methods of molecular cytogenetics in pre- and postnatal diagnosis of chromosome aberrations]. Klin Lab Diagn (2000) 0.76
[Chromosome abnormalities in schizophrenia]. Zh Nevrol Psikhiatr Im S S Korsakova (2006) 0.76
Fluorescence intensity profiles of in situ hybridization signals depict genome architecture within human interphase nuclei. Tsitol Genet (2009) 0.76
[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
[Molecular cytogenetic methods for studying interphase chromosomes in human brain cells]. Genetika (2010) 0.75
Identification of marker chromosomes by in situ hybridization technique using alpha and "classical" satellite DNA probes with relative chromosomal specificity. Tsitol Genet (1994) 0.75
[Quantitative analysis of fluorescence in situ hybridization (FISH) signals for molecular cytogenetic diagnosis]. Klin Lab Diagn (2005) 0.75
[Integration of the recipient's genome by transplanted cells of the donor bone marrow]. Klin Lab Diagn (2003) 0.75
[Chromosomal anomalies in children with undifferentiated forms of metal retardation based on molecular cytogenetic research data]. Tsitol Genet (1994) 0.75
[Dynamic bone marrow take and lymphohematopoietic chimerism following allogeneic bone marrow transplantation]. Ter Arkh (1995) 0.75
[Liposomal daunorubicin and interferon-alfa in combination with all-retinoic acid--a new regime for the treatment of acute promyelocytic leukemia]. Ter Arkh (2002) 0.75
[Contemporary views on Rett's syndrome: clinical, cytogenetic and molecular studies]. Zh Nevrol Psikhiatr Im S S Korsakova (1999) 0.75
[Molecular cytogenetic studies of chromosomal abnormalities and disorders in nervous and mental diseases: search for biological markers for diagnosis]. Vestn Ross Akad Med Nauk (2001) 0.75
Enlargement of the long arm of a B-group chromosome (Bq+) in a boy aged nine years. Sov Genet (1973) 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
[Cytogenetic and molecular genetic diagnostics of Rett syndrome in children]. Zh Nevrol Psikhiatr Im S S Korsakova (1998) 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
[Combination of interferon-alpha and all-trans-retinoic acid as a treatment for maintaining remission in high-risk group patients with acute myeloid leukemia]. Ter Arkh (2001) 0.75
[Detection of autoantibodies to neutrophils in patients with immune (hapten) agranulocytosis]. Klin Lab Diagn (2003) 0.75
[Effectiveness of allogeneic bone marrow transplantation in patients with acute leukemia in complete remission and in patients with chronic myeloid leukemia during the chronic phase]. Ter Arkh (1999) 0.75
[Allogenic bone marrow transplantation after reduced intensity conditioning regimens in therapy of patients with hemoblastoses]. Ter Arkh (2003) 0.75
[Amplification of hypervariable genomic regions for establishment of the type of hematopoiesis in hemoblastosis patients after allogeneic bone marrow transplantation]. Genetika (1997) 0.75
[Nervous and mental diseases in boys and mutations in MECP2 gene]. Zh Nevrol Psikhiatr Im S S Korsakova (2004) 0.75
[Unusual case of 18p- syndrome: diagnosis using a cloned DNA fragment]. Tsitol Genet (1986) 0.75
[The biological characteristics and treatment of acute promyelocytic leukemia]. Ter Arkh (1998) 0.75
[Molecular cytogenetic study of Robertsonian translocation 13;14 and Down syndrome in a 3-year-old infant]. Tsitol Genet (2005) 0.75
[The efficacy of high-dose chemotherapy and the transplantation of autologous hemopoietic cells in lymphogranulomatosis]. Ter Arkh (2000) 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
[The induction of the antitumor activity of T-lymphocytes by antigen-presenting cells obtained from the blast cells of patients with acute leukemias]. Ter Arkh (2000) 0.75
[Experience in using the new antiemetic preparation Navoban in hemoblastosis patients]. Ter Arkh (1993) 0.75
[Chromosomal diseases in children]. Med Sestra (1988) 0.75
[Effectiveness of trans-retinoic acid in the treatment of acute promyelocytic leukemia: initial results of a multicenter study]. Ter Arkh (1999) 0.75
[Instability of chromosomes in human nerve cells (normal and with neuromental diseases)]. Genetika (2010) 0.75
[Molecular-cytogenetic diagnosis of hereditary diseases associated with diverse anomalies of X chromosome]. Pediatriia (1989) 0.75
[Genomic instability in the brain: etiology, pathogenesis and new biological markers of psychiatric disorders]. Vestn Ross Akad Med Nauk (2012) 0.75