Suspected microdeletion syndromes and molecular cytogenetic techniques: an experience with 330 cases

Antzeko izenburuak

• Fluorescence in situ hybridization (FISH) using non-commercial probes in the diagnosis of clinically suspected microdeletion syndromes
  nork: Halder, Ashutosh, et al.
  Argitaratua: (2013)
• SNP Microarray in FISH Negative Clinically Suspected 22q11.2 Microdeletion Syndrome
  nork: Halder, Ashutosh, et al.
  Argitaratua: (2016)
• Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size
  nork: Halder, Ashutosh, et al.
  Argitaratua: (2012)
• Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India
  nork: Halder, Ashutosh, et al.
  Argitaratua: (2010)
• Rapid detection of chromosome X, Y, 13, 18, and 21 aneuploidies by primed in situ labeling/synthesis technique
  nork: Halder, Ashutosh, et al.
  Argitaratua: (2013)