Haan EA - Search Results

1

Umbilical cord ulceration in association with intestinal atresia in a child with deletion 13q and Hirschsprung's disease.

Khong TY, Ford WD, Haan EA. Khong TY, et al. Among authors: haan ea. Arch Dis Child Fetal Neonatal Ed. 1994 Nov;71(3):F212-3. doi: 10.1136/fn.71.3.f212. Arch Dis Child Fetal Neonatal Ed. 1994. PMID: 7820720 Free PMC article.

2

First-trimester diagnosis of Smith-Lemli-Opitz syndrome.

Sharp P, Haan E, Fletcher JM, Khong TY, Carey WF. Sharp P, et al. Prenat Diagn. 1997 Apr;17(4):355-61. doi: 10.1002/(sici)1097-0223(199704)17:4<355::aid-pd78>3.0.co;2-m. Prenat Diagn. 1997. PMID: 9160388

3

Genetic susceptibility to viral exposure may increase the risk of cerebral palsy.

Djukic M, Gibson CS, Maclennan AH, Goldwater PN, Haan EA, McMichael G, Priest K, Dekker GA, Hague WM, Chan A, Rudzki Z, VAN Essen P, Khong TY, Morton MR, Ranieri E, Scott H, Tapp H, Casey G. Djukic M, et al. Among authors: haan ea. Aust N Z J Obstet Gynaecol. 2009 Jun;49(3):247-53. doi: 10.1111/j.1479-828X.2009.00999.x. Aust N Z J Obstet Gynaecol. 2009. PMID: 19566553

4

Lung disease associated with periventricular nodular heterotopia and an FLNA mutation.

Masurel-Paulet A, Haan E, Thompson EM, Goizet C, Thauvin-Robinet C, Tai A, Kennedy D, Smith G, Khong TY, Solé G, Guerineau E, Coupry I, Huet F, Robertson S, Faivre L. Masurel-Paulet A, et al. Eur J Med Genet. 2011 Jan-Feb;54(1):25-8. doi: 10.1016/j.ejmg.2010.09.010. Epub 2010 Oct 1. Eur J Med Genet. 2011. PMID: 20888935

5

A familial cryptic subtelomeric deletion 12p with variable phenotypic effect.

Baker E, Hinton L, Callen DF, Haan EA, Dobbie A, Sutherland GR. Baker E, et al. Among authors: haan ea. Clin Genet. 2002 Mar;61(3):198-201. doi: 10.1034/j.1399-0004.2002.610305.x. Clin Genet. 2002. PMID: 12000361

6

Perinatal risk factors for developmental dysplasia of the hip.

Chan A, McCaul KA, Cundy PJ, Haan EA, Byron-Scott R. Chan A, et al. Among authors: haan ea. Arch Dis Child Fetal Neonatal Ed. 1997 Mar;76(2):F94-100. doi: 10.1136/fn.76.2.f94. Arch Dis Child Fetal Neonatal Ed. 1997. PMID: 9135287 Free PMC article.

7

High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.

Fang YY, Bain S, Haan EA, Eyre HJ, MacDonald M, Wright TJ, Altherr MR, Riess O, Sutherland G, Callen DF. Fang YY, et al. Among authors: haan ea. Am J Med Genet. 1997 Sep 5;71(4):453-7. Am J Med Genet. 1997. PMID: 9286454

8

The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.

Callen DF, Freemantle CJ, Ringenbergs ML, Baker E, Eyre HJ, Romain D, Haan EA. Callen DF, et al. Among authors: haan ea. Am J Hum Genet. 1990 Sep;47(3):493-8. Am J Hum Genet. 1990. PMID: 2393023 Free PMC article.

9

Origins of accessory small ring marker chromosomes derived from chromosome 1.

Callen DF, Eyre H, Fang YY, Guan XY, Veleba A, Martin NJ, McGill J, Haan EA. Callen DF, et al. Among authors: haan ea. J Med Genet. 1999 Nov;36(11):847-53. J Med Genet. 1999. PMID: 10544230 Free PMC article.

10

Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.

Haan EA, Hull YJ, White S, Cockington R, Charlton P, Callen DF. Haan EA, et al. Am J Med Genet. 1989 Apr;32(4):490-4. doi: 10.1002/ajmg.1320320412. Am J Med Genet. 1989. PMID: 2773990

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