Goldblatt J - Search Results

1

Population screening for cystic fibrosis in Western Australia: community response.

Honnor M, Zubrick SR, Walpole I, Bower C, Goldblatt J. Honnor M, et al. Among authors: goldblatt j. Am J Med Genet. 2000 Jul 31;93(3):198-204. doi: 10.1002/1096-8628(20000731)93:3<198::aid-ajmg7>3.0.co;2-q. Am J Med Genet. 2000. PMID: 10925381

2

Mutation analysis of Western Australian families affected by cystic fibrosis.

Goldblatt J, Creegan R, Edkins T, Landau LI, Ryan G, Walpole IR. Goldblatt J, et al. Med J Aust. 1995 Jan 2;162(1):12-5. doi: 10.5694/j.1326-5377.1995.tb138402.x. Med J Aust. 1995. PMID: 7845290

3

Evaluation of a project to enhance knowledge of hereditary diseases and management.

Walpole IR, Watson C, Moore D, Goldblatt J, Bower C. Walpole IR, et al. Among authors: goldblatt j. J Med Genet. 1997 Oct;34(10):831-7. doi: 10.1136/jmg.34.10.831. J Med Genet. 1997. PMID: 9350816 Free PMC article.

4

Craniosynostosis in Western Australia, 1980-1994: a population-based study.

Singer S, Bower C, Southall P, Goldblatt J. Singer S, et al. Among authors: goldblatt j. Am J Med Genet. 1999 Apr 23;83(5):382-7. doi: 10.1002/(sici)1096-8628(19990423)83:5<382::aid-ajmg8>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10232748

5

Deletion of 8p23.1 with features of Cornelia de Lange syndrome and congenital diaphragmatic hernia and a review of deletions of 8p23.1 to 8pter? A further locus for Cornelia de Lange syndrome.

Baynam G, Goldblatt J, Walpole I. Baynam G, et al. Among authors: goldblatt j. Am J Med Genet A. 2008 Jun 15;146A(12):1565-70. doi: 10.1002/ajmg.a.32095. Am J Med Genet A. 2008. PMID: 18470924 Review.

6

Rapp-Hodgkin hypohidrotic ectodermal dysplasia syndrome.

Walpole IR, Goldblatt J. Walpole IR, et al. Among authors: goldblatt j. Clin Genet. 1991 Feb;39(2):114-20. doi: 10.1111/j.1399-0004.1991.tb02996.x. Clin Genet. 1991. PMID: 2015692 Review.

7

Autosomal dominant osteopetrosis type II with "malignant" presentation: further support for heterogeneity?

Walpole IR, Nicoll A, Goldblatt J. Walpole IR, et al. Among authors: goldblatt j. Clin Genet. 1990 Oct;38(4):257-63. doi: 10.1111/j.1399-0004.1990.tb03578.x. Clin Genet. 1990. PMID: 2268972

8

Dandy-Walker malformation (variant), cystic dysplastic kidneys, and hepatic fibrosis: a distinct entity or Meckel syndrome?

Walpole IR, Goldblatt J, Hockey A, Knowles S. Walpole IR, et al. Among authors: goldblatt j. Am J Med Genet. 1991 Jun 1;39(3):294-8. doi: 10.1002/ajmg.1320390310. Am J Med Genet. 1991. PMID: 1867280

9

The limitation of referral level fetal ultrasound examination in the detection of spina bifida in Western Australia, 1990-1991.

Walpole IR, Phillips J, Pemberton PJ, Bower C, Goldblatt J. Walpole IR, et al. Among authors: goldblatt j. Med J Aust. 1993 Oct 4;159(7):441-4. doi: 10.5694/j.1326-5377.1993.tb137960.x. Med J Aust. 1993. PMID: 7692226

10

Genetic counselling and gene mutation analysis in familial adenomatous polyposis in Western Australia.

Walpole IR, Kool DA, Edkins T, Creegan R, Levitt S, Francis ST, Goldblatt J. Walpole IR, et al. Among authors: goldblatt j. Med J Aust. 1995 May 1;162(9):464-7. doi: 10.5694/j.1326-5377.1995.tb140006.x. Med J Aust. 1995. PMID: 7746201

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