Advanced search
Publication Cover
Journal of Obstetrics and Gynaecology Volume 34, 2014 - Issue 2
Submit an article Journal homepage
131
Views
3
CrossRef citations to date
0
Altmetric
Research Article

Prenatal diagnosis and molecular cytogenetic characterisation of a de novo 18p deletion

G. FoguClinical Genetics, Department of Biomedical Sciences
,
G. CapobiancoGynaecologic and Obstetric Clinic, Department of Surgical, Microsurgical and Medical SciencesCorrespondence[email protected]
,
F. CambosuClinical Genetics, Department of Biomedical Sciences
,
P. BandieraDepartment of Biomedical Sciences, Division of Human Anatomy, University of Sassari, Italy
,
A. PirinoDepartment of Biomedical Sciences, Division of Human Anatomy, University of Sassari, Italy
,
M. A. MoroClinical Genetics, Department of Biomedical Sciences
,
P. M. CampusClinical Genetics, Department of Biomedical Sciences
,
G. SoroDepartment of Biomedical Sciences, Division of Human Anatomy, University of Sassari, Italy
,
M. DessoleGynaecologic and Obstetric Clinic, Department of Surgical, Microsurgical and Medical Sciences
&
A. MontellaDepartment of Biomedical Sciences, Division of Human Anatomy, University of Sassari, Italy
 show all
Pages 192-193 | Published online: 23 Jan 2014

References

  • Cohen MM Jr. 2006. Holoprosencephaly: clinical, anatomic, and molecular dimensions. Birth Defects Research. Part A, Clinical and Molecular Teratology 76:658–673.
  • Jones KL. 2006. Deletion 18p syndrome. In Smith's recognizable pattern of human malformation. 6th ed. Philadelphia: Elsevier Saunders. p. 60–61.
  • Kim YM, Cho EH, Kim JM et al. 2004. Del(18p) syndrome with increased nuchal translucency in prenatal diagnosis. Prenatal Diagnosis 24:161–164.
  • Nicolaides KH, Brizot ML, Snijders RJ. 1994. Fetal nuchal translucency: ultrasound screening for fetal trisomies in the first trimester of pregnancy. British Journal of Obstetrics and Gynaecology 101:782–786.
  • Tharapel AT, Qumsiyeh MB, Martens PR et al. 1991. Identification of the origin of centromeres in whole arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes. American Journal of Medical Genetics 40:117–120.
  • Thieffry S, Arthuis M, de Grouchy J et al. 1963. Deletion of the short arms of chromosome 17–18: complex deformities with oligophrenia. Archives Francaises de Pediatrie 20:740–745.
  • Turleau C. 2008. Monosomy 18p. Orphanet Journal of Rare Diseases 3:4–5.
  • Wang JC, Nemana L, Kou S et al. 1997. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p. American Journal of Medical Genetics 71:463–466.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.