Molecular Cytogenetics View Homepage


Ontology type: schema:Periodical      Open Access: True


Journal Info

START YEAR

2008

PUBLISHER

BioMed Central

LANGUAGE

en

HOMEPAGE

http://molecularcytogenetics.biomedcentral.com/

Recent publications latest 20 shown

  • 2019-12 Chromoanagenesis: cataclysms behind complex chromosomal rearrangements
  • 2019-12 Discrepancy of QF-PCR, CMA and karyotyping on a de novo case of mosaic isodicentric Y chromosomes
  • 2018-12 Investigation of copy number variations on chromosome 21 detected by comparative genomic hybridization (CGH) microarray in patients with congenital anomalies
  • 2018-12 Can telomere shortening be the main indicator of non-viable fetus elimination?
  • 2018-12 Novel phenotype of 5p13.3-q11.2 duplication resulting from supernumerary marker chromosome 5: implications for management and genetic counseling
  • 2018-12 Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant
  • 2018-12 The decision on the embryo to transfer after Preimplantation Genetic Diagnosis for X-autosome reciprocal translocation in male carrier
  • 2018-12 Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies
  • 2018-12 A foetus with 18p11.32-q21.2 duplication and Xp22.33-p11.1 deletion derived from a maternal reciprocal translocation t(X;18)(q13;q21.3)
  • 2018-12 Parental origin of deletions and duplications – about the necessity to check for cryptic inversions
  • 2018-12 Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia
  • 2018-12 Distinct subtypes of genomic PTEN deletion size influence the landscape of aneuploidy and outcome in prostate cancer
  • 2018-12 Characterization of chromosome composition of sugarcane in nobilization by using genomic in situ hybridization
  • 2018-12 Application of chromosomal microarray analysis in products of miscarriage
  • 2018-12 A feasible diagnostic approach for the translocation carrier from the indication of products of conception
  • 2018-12 Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22
  • 2018-12 An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia
  • 2018-12 A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy – case report and review of the literature
  • 2018-12 An improved method for inducing prometaphase chromosomes in plants
  • 2018-12 Publisher Correction: Is DNA methylation the new guardian of the genome?
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