Refining the critical region for congenital diaphragmatic hernia on chromosome 15q26 from the study of four fetuses

This publication has 19 references indexed in Scilit:

• Terminal 6.9 Mb deletion of chromosome 15q, associated with a structurally abnormal X chromosome in a patient with congenital diaphragmatic hernia and heart defect
  European Journal of Medical Genetics, 2011
• Clinical and Functional Characteristics of a Novel Heterozygous Mutation of theIGF1RGene and IGF1R Haploinsufficiency due to Terminal 15q26.2->qter Deletion in Patients with Intrauterine Growth Retardation and Postnatal Catch-Up Growth Failure
  The Journal of Clinical Endocrinology & Metabolism, 2011
• Gene expression in the developing diaphragm: significance for congenital diaphragmatic hernia
  American Journal of Physiology-Lung Cellular and Molecular Physiology, 2008
• Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: Two patients and review of the literature
  American Journal of Medical Genetics Part A, 2007
• Genetic Factors in Congenital Diaphragmatic Hernia
  The American Journal of Human Genetics, 2007
• Congenital diaphragmatic hernia associated with duplication of 11q23‐qter
  American Journal of Medical Genetics Part A, 2006
• Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization
  The American Journal of Human Genetics, 2005
• Association of Deletions of the Chromosomal Region 15q24-ter and Diaphragmatic Hernia: A New Case and Discussion of the Literature
  Fetal Diagnosis and Therapy, 2004
• Congenital diaphragmatic hernia: Is 15q26.1‐26.2 a candidate locus?
  American Journal of Medical Genetics Part A, 2003
• Congenital diaphragmatic hernia in a family segregating a reciprocal translocation t(5;15)(p15.3;q24)
  American Journal of Medical Genetics, 2000