Viewing StudyNCT00032877



Ignite Creation Date: 2024-05-05 @ 11:25 AM
Last Modification Date: 2024-10-26 @ 9:07 AM
Study NCT ID: NCT00032877
Status: COMPLETED
Last Update Posted: 2008-03-04
First Post: 2002-04-04

Brief Title: Genetic Analysis of Fraser Syndrome and Fryns Syndrome
Sponsor: National Human Genome Research Institute NHGRI
Organization: National Institutes of Health Clinical Center CC

Conditions & Keywords Data

Conditions:
Name
Abnormalities Multiple
Fraser Syndrome
Fryns Syndrome
Chromosomal Abnormalities
Keywords:
Name View
Positional Cloning View
Linkage Study View
Gene Identification Study View
Diaphragmatic Hernia View
Fraser Syndrome View
Cryptophthalmos View
Fryns Syndrome View
Hydrolethalus Syndrome View