Chromosomal deletion 4p15.32→p14 in a treacher collins syndrome patient: Exclusion of the disease locus from and mapping of anonymous DNA sequences to this region

This publication has 13 references indexed in Scilit:

• The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome
  Human Genetics, 1990
• Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms pp. 622-643
  Cytogenetic and Genome Research, 1989
• A new family of mouse homeo box-containing genes: molecular structure, chromosomal location, and developmental expression of Hox-7.1.
  Genes & Development, 1989
• Anthropometric evaluation of dysmorphology in craniofacial anomalies: Treacher Collins syndrome
  American Journal of Physical Anthropology, 1987
• Isolation of polymorphic DNA fragments from human chromosome 4
  Nucleic Acids Research, 1987
• Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf–Hirschhorn syndrome
  Nature, 1985
• Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase B
  Human Genetics, 1983
• Older paternal age and fresh gene mutation: Data on additional disorders
  The Journal of Pediatrics, 1975
• Mandibulo-Facial Dysostosis
  American Journal of Diseases of Children, 1967
• Dysostosis Mandibulo-Facialis
  The Journal of Laryngology & Otology, 1963