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PMID: 8773902 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The search for hemizygosity at 22qll in patients with isolated cleft palate.

Journal of craniofacial genetics and developmental biology ·Vol. 16 ·No. 2 ·1996-00-00 ·Pages 118-21

Mingarelli R, Digilio MC, Mari A, Amati F, Standoli L, Giannotti A, Novelli G, Dallapiccola B

Abstract

The striking association between oral clefting and the velocardio-facial syndrome (VCFS), a common disorder pathogenetically related to 22q11 deficiency, has prompted the search for this deletion in a group of patients with isolated cleft palate. (CP). Thirty-three patients with posterior CP and 5 with complete CP were included in this study, together with 12 patients with a clinical diagnosis of VCFS. Standard and high resolution chromosome analysis was performed, providing normal results. Southern blotting followed by densitometric analysis and fluorescent in situ hydridization of region 22q11 showed no single case of deletion among the isolated CP patients, while deficiency was found in 10 of 12 VCFS patients. These results demonstrate that hemizygosity at 22q11 is not increased in isolated CP.

MeSH Terms
Adolescent Blotting, Southern Child Child, Preschool Chromosome Deletion Chromosomes, Human, Pair 22 Cleft Palate/genetics Densitometry Face/abnormalities Female Heart Defects, Congenital/genetics Homozygote Humans In Situ Hybridization, Fluorescence Infant Infant, Newborn Male Syndrome
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Mingarelli R
Department of Public Health and Cell Biology, Tor Vergata University, Rome, Italy.
Digilio M C
Mari A
Amati F
Standoli L
Giannotti A
Novelli G
Dallapiccola B
Article Info
Journal
Journal of craniofacial genetics and developmental biology
Abbr.
J Craniofac Genet Dev Biol
ISSN
0270-4145
Published
1996-00-00
Pages
118-21
Language
English
Region
Denmark
NLM ID
8109845
Subset
IM
External Links
PubMed source
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