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E A Haan

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Articles 96
Citations 956
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Recent Articles
1.
OCallaghan M, MacLennan A, Haan E, Dekker G
Hum Genet . 2009 Feb; 126(1):149-72. PMID: 19238444
Cerebral palsy has been associated with a number of candidate genes. To date, no systematic review has been conducted to synthesise genetic polymorphism associations with cerebral palsy. We apply the...
2.
Gibson C, Goldwater P, MacLennan A, Haan E, Priest K, Dekker G
BJOG . 2008 Feb; 115(4):492-500. PMID: 18271886
Objective: To investigate the role of fetal viral infection in the development of a range of adverse pregnancy outcomes (APOs), including pregnancy-induced hypertensive disorders (PIHD), antepartum haemorrhage (APH), birthweight <10th...
3.
Ades L, Sullivan K, Biggin A, Haan E, Brett M, Holman K, et al.
Am J Med Genet A . 2006 Apr; 140(10):1047-58. PMID: 16596670
The recent identification of TGFBR2 mutations in Marfan syndrome II (MFSII) [Mizuguchi et al. (2004); Nat Genet 36:855-860] and of TGFBR1 and TGFBR2 mutations in Loeys-Dietz aortic aneurysm syndrome (LDS)...
4.
Field M, Grattan-Smith P, Piper S, Thompson E, Haan E, Edwards M, et al.
Am J Med Genet A . 2003 Sep; 122A(1):6-12. PMID: 12949965
PEHO syndrome is a rare progressive infantile encephalopathy with onset within the first few months of life. Few patients fulfilling the diagnostic criteria for PEHO syndrome have been reported outside...
5.
Baker E, Hinton L, Callen D, Haan E, Dobbie A, Sutherland G
Clin Genet . 2002 May; 61(3):198-201. PMID: 12000361
A 15-year-old-boy and his mother, both carrying a cryptic deletion within 12p13.33, are described. The proband has a mild phenotype with moderate mental retardation and severe behavioural problems. The mother...
6.
Kelberman D, Tyson J, Chandler D, McInerney A, Slee J, Albert D, et al.
Hum Genet . 2002 Jan; 109(6):638-45. PMID: 11810276
Hemifacial microsomia (HFM) is a common birth defect involving first and second branchial arch derivatives. The phenotype is extremely variable. In addition to craniofacial anomalies there may be cardiac, vertebral...
7.
Ryall R, Callen D, Cocciolone R, Duvnjak A, Esca R, Frantzis N, et al.
Prenat Diagn . 2001 Aug; 21(7):553-7. PMID: 11494290
Of the 65 328 pregnancies of South Australian mothers screened by the South Australian Maternal Serum Antenatal Screening (SAMSAS) Programme between 1 January 1991 and 31 December 1997, 3431 (5.25%)...
8.
Cheffins T, Chan A, Haan E, Ranieri E, Ryall R, Keane R, et al.
BJOG . 2001 Feb; 107(12):1453-9. PMID: 11192100
Objectives: To describe the impact of maternal serum screening on the birth prevalence of Down's syndrome and on the use of amniocentesis and chorionic villus sampling in South Australia. Design:...
9.
Chan A, Haan E
Med J Aust . 2000 Sep; 173(4):223. PMID: 11008602
No abstract available.
10.
Hocking T, Feichtinger W, Schmid M, Haan E, Baker E, Sutherland G
Chromosome Res . 1999 Dec; 7(7):553-6. PMID: 10598570
Homozygotes for the rare folate-sensitive autosomal fragile sites have never been recorded. Two non-folate-sensitive rare fragile sites (FRA10B and FRA17A) have been previously recorded in normal individuals. We document two...