The Western Australian Family Connections Genealogical Project: Detection of familial occurrences of single gene and chromosomal disorders

The Western Australian Family Connections Genealogical Project: Detection of familial occurrences of single gene and chromosomal disorders

Aim: To investigate using a Western Australian (WA) genealogical database for the identification of single gene and chromosome disorders among families. Method: Hospital admissions for single gene and chromosome disorders recorded during 2000–2006 were identified from the WA Hospital Morbidity Data...

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Bibliographic Details
Main Authors: Brameld, Kate, Dye, Danielle, Maxwell, Susannah, Brisbane, Joanna, Glasson, Emma, Goldblatt, Jack, O'Leary, Peter
Format: Journal Article
Published: Mary Ann Liebert, Inc. Publishers 2014
Subjects:
tuberous sclerosis
cystic fibrosis
osteogenesis imperfecta
WA Hospital Morbidity Data System
myotonic dystrophies
Von Willebrand’s disease
Factor VIII deficiency
neurofibromatosis
single gene
WA Family Connections Genealogical Project
chromosome disorders
Online Access:http://hdl.handle.net/20.500.11937/33584

Internet

http://hdl.handle.net/20.500.11937/33584

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