Interstitial deletions without phenotypic effect: Prenatal diagnosis of a new family and brief review

This publication has 12 references indexed in Scilit:

• Tricho‐rhino‐phalangeal and branchio‐oto syndromes in a family with an inherited rearrangement of chromosome 8q
  American Journal of Medical Genetics, 1989
• The Human Gene Mapping Workshops in transition
  Cytogenetic and Genome Research, 1989
• Deletion of a single chromosome band 4q26 in a malformed girl: exclusion of Rieger syndrome associated gene(s) from the 4q26 segment.
  Journal of Medical Genetics, 1988
• Gene-rich chromosome regions and autosomal trisomy
  Human Genetics, 1987
• 8q24.12 Interstitial deletion in trichorhinophalangeal syndrome type I
  Human Genetics, 1986
• The size of prometaphase chromosome segments Tables using percentages of haploid autosome length (750 band stage
  Clinical Genetics, 1985
• Deletion of band 13q21 is compatible with normal phenotype
  Human Genetics, 1985
• The effect of oxygen tension on colony formation and cell proliferation of amniotic fluid cellsin vitro
  Prenatal Diagnosis, 1984
• Structural differences in reciprocal translocations
  Human Genetics, 1979
• Systematic analysis of 95 reciprocal translocations of autosomes
  Human Genetics, 1978