Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review

Lignende værker

• Identification and clinical evaluation of segments of homozygosity, uniparental disomy and complex chromosomal abnormalities revealed by copy-number SNP arrays
  af: Wang, Jia-Chi, et al.
  Udgivet: (2014)
• Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory
  af: Wang, Boris T, et al.
  Udgivet: (2014)
• Neocentric X-chromosome in a girl with Turner-like syndrome
  af: Hemmat, Morteza, et al.
  Udgivet: (2012)
• Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving DOCK8, KANK1, EHMT1 genes identified by using high-resolution oligonucleotide-single nucleotide polymorphism array analysis
  af: Wang, Jia-Chi, et al.
  Udgivet: (2016)
• Isochromosome Yp and jumping translocation of Yq resulting in five cell lines in an infertile male: a case report and review of the literature
  af: Hemmat, Morteza, et al.
  Udgivet: (2013)