High population incidence of the 15p marker D15Z1 mapping to the short arm of one homologue 14

No abstract is available for this paper.

• Publication year

  2004

• Venue

  Human Genetics

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/BF00197281PMID 1733844
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes

  2005cited by this paper
• Organization of a repetitive human 1.8 kb KpnI sequence localized in the heterochromatin of chromosome 15

  2005cited by this paper

• Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples

  2019cites this paper
• Translocaciones crípticas de cromosomas acrocéntricos en muestras de tejido de aborto aneuploide

  2015cites this paper
• Acrocentric bivalents positioned preferentially nearby to the XY pair in metaphase I human spermatocytes.

  2012cites this paper
• Interchromosomal effect analyses by sperm FISH: incidence and distribution among reorganization carriers

  2011cites this paper
• Distribution of the D15Z1 copy number polymorphism

  2007cites this paper
• Behaviour of human heterochromatic regions during the synapsis of homologous chromosomes.

  2006cites this paper
• Fractionation of chromosome 15 with an affinity-based approach using magnetic beads.

  2006cites this paper
• A DA/DAPI positive human 14p heteromorphism defined by fluorescence in-situ hybridisation using chromosome 15-specific probes D15Z1 (satellite III) and p-TRA-25 (alphoid).

  2004cites this paper
• Chromosome 15p marker D15Z1 frequently maps to the short arm of other D-group chromosomes

  2004cites this paper
• Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs)

  2004cites this paper
• Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.

  1997cites this paper
• Human satellites 2 and 3.

  1994cites this paper
• Moving satellites and unstable chromosome translocations: clinical and cytogenetic implications.

  1993cites this paper
• Molecular cytogenetic characterization of three familial cases of satellited Y chromosomes

  1993cites this paper
• Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome

  1993cites this paper
• A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.

  1992cites this paper
• Molecular cytogenetics of Prader-Willi and Angelman syndromes.

  1992cites this paper