Haan E - Search Results

1

Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa-Kuroki) syndrome.

White SM, Thompson EM, Kidd A, Savarirayan R, Turner A, Amor D, Delatycki MB, Fahey M, Baxendale A, White S, Haan E, Gibson K, Halliday JL, Bankier A. White SM, et al. Among authors: haan e. Am J Med Genet A. 2004 Jun 1;127A(2):118-27. doi: 10.1002/ajmg.a.20674. Am J Med Genet A. 2004. PMID: 15108197

2

Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers.

Mulley JC, Gedeon AK, White SJ, Haan EA, Richards RI. Mulley JC, et al. Among authors: haan ea. J Med Genet. 1991 Jul;28(7):448-52. doi: 10.1136/jmg.28.7.448. J Med Genet. 1991. PMID: 1895314 Free PMC article.

3

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

4

Familial occurrence of Brachmann-de Lange syndrome.

Bankier A, Haan E, Birrell R. Bankier A, et al. Among authors: haan e. Am J Med Genet. 1986 Sep;25(1):163-5. doi: 10.1002/ajmg.1320250119. Am J Med Genet. 1986. PMID: 3799716 No abstract available.

5

Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity.

Chenevix-Trench G, Wicking C, Berkman J, Sharpe H, Hockey A, Haan E, Oley C, Ravine D, Turner A, Goldgar D, et al. Chenevix-Trench G, et al. Among authors: haan e. Am J Hum Genet. 1993 Sep;53(3):760-7. Am J Hum Genet. 1993. PMID: 8352281 Free PMC article.

6

Prenatal exposure to phenytoin, facial development, and a possible role for vitamin K.

Howe AM, Lipson AH, Sheffield LJ, Haan EA, Halliday JL, Jenson F, David DJ, Webster WS. Howe AM, et al. Among authors: haan ea. Am J Med Genet. 1995 Sep 11;58(3):238-44. doi: 10.1002/ajmg.1320580309. Am J Med Genet. 1995. PMID: 8533825 Review.

7

Clinical features in 27 patients with Angelman syndrome resulting from DNA deletion.

Smith A, Wiles C, Haan E, McGill J, Wallace G, Dixon J, Selby R, Colley A, Marks R, Trent RJ. Smith A, et al. Among authors: haan e. J Med Genet. 1996 Feb;33(2):107-12. doi: 10.1136/jmg.33.2.107. J Med Genet. 1996. PMID: 8929945 Free PMC article. Review.

8

Mutation detection in FGFR2 craniosynostosis syndromes.

Hollway GE, Suthers GK, Haan EA, Thompson E, David DJ, Gecz J, Mulley JC. Hollway GE, et al. Among authors: haan ea. Hum Genet. 1997 Feb;99(2):251-5. doi: 10.1007/s004390050348. Hum Genet. 1997. PMID: 9048930

9

Clinical features in four patients with Angelman syndrome resulting from paternal uniparental disomy.

Smith A, Marks R, Haan E, Dixon J, Trent RJ. Smith A, et al. Among authors: haan e. J Med Genet. 1997 May;34(5):426-9. doi: 10.1136/jmg.34.5.426. J Med Genet. 1997. PMID: 9152844 Free PMC article.

10

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

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