3p− syndrome defines a hearing loss locus in 3p25.3

This publication has 40 references indexed in Scilit:

• Submicroscopic Deletion in Patients with Williams-Beuren Syndrome Influences Expression Levels of the Nonhemizygous Flanking Genes
  American Journal of Human Genetics, 2006
• Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non‐syndromic hearing impairment
  Clinical Genetics, 2004
• Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion
  Human Genetics, 2004
• Changes in Cytochemistry of Sensory and Nonsensory Cells in Gentamicin-Treated Cochleas
  Journal of the Association for Research in Otolaryngology, 2003
• Functional Study of GJB2 in Hereditary Hearing Loss
  The Laryngoscope, 2002
• 46, XY, del (3) (pter→p25) syndrome: further delineation of the clinical phenotype
  European Journal of Pediatrics, 1999
• mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw)
  Genomics, 1997
• Molecular genetic analysis of the 3p — syndrome
  Human Molecular Genetics, 1994
• Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: Karyotype‐phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3
  American Journal of Medical Genetics, 1990
• A second patient with partial deletion of the short arm of chromosome 3: karyotype 46,XY,del(3)(p25).
  Journal of Medical Genetics, 1982