Chitayat D - Search Results

1

PGD for a carrier of an intrachromosomal insertion using aCGH.

Jones CA, Kolomietz E, Maire G, Vlasschaert M, Joseph-George AM, Myles-Reid D, Chong K, Chitayat D, Arthur R. Jones CA, et al. Among authors: chitayat d. Syst Biol Reprod Med. 2014 Dec;60(6):377-82. doi: 10.3109/19396368.2014.962710. Epub 2014 Sep 23. Syst Biol Reprod Med. 2014. PMID: 25247722 Review.

2

Functional disomy of Xp: prenatal findings and postnatal outcome.

Kolomietz E, Godbole K, Winsor EJ, Stockley T, Seaward G, Chitayat D. Kolomietz E, et al. Among authors: chitayat d. Am J Med Genet A. 2005 May 1;134(4):393-8. doi: 10.1002/ajmg.a.30652. Am J Med Genet A. 2005. PMID: 15793841

3

Array-based genomic delineation of a familial duplication 11q14.1-q22.1 associated with recurrent depression.

Kolomietz E, Ben-Omran T, Chitayat D, Mah M, Murphy J, Nie G, Teshima I. Kolomietz E, et al. Among authors: chitayat d. Am J Med Genet B Neuropsychiatr Genet. 2006 Apr 5;141B(3):214-9. doi: 10.1002/ajmg.b.30297. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16526031

4

X-Linked dominant chondrodysplasia punctata: prenatal diagnosis and autopsy findings.

Umranikar S, Glanc P, Unger S, Keating S, Fong K, Trevors CD, Myles-Reid D, Chitayat D. Umranikar S, et al. Among authors: chitayat d. Prenat Diagn. 2006 Dec;26(13):1235-40. doi: 10.1002/pd.1594. Prenat Diagn. 2006. PMID: 17086568

5

Fatal lung fibrosis associated with immunodeficiency and gonadal dysgenesis in 46XX sisters--a new syndrome.

Somech R, Somers GR, Chitayat D, Grunebaum E, Atkinson A, Kolomietz E, Roifman CM. Somech R, et al. Among authors: chitayat d. Am J Med Genet A. 2008 Jan 1;146A(1):8-14. doi: 10.1002/ajmg.a.32014. Am J Med Genet A. 2008. PMID: 17937424

6

Acrofacial dysostosis syndrome type Rodriguez: prenatal diagnosis and autopsy findings.

Sermer D, Quercia N, Chong K, Chitayat D. Sermer D, et al. Among authors: chitayat d. Am J Med Genet A. 2007 Dec 15;143A(24):3286-9. doi: 10.1002/ajmg.a.32021. Am J Med Genet A. 2007. PMID: 18000904

7

Raine syndrome: a rare lethal osteosclerotic bone dysplasia. Prenatal diagnosis, autopsy, and neuropathological findings.

Chitayat D, Shannon P, Keating S, Toi A, Blaser S, Friedberg T, Superti-Furga A, Chong K, Unger S. Chitayat D, et al. Am J Med Genet A. 2007 Dec 15;143A(24):3280-5. doi: 10.1002/ajmg.a.32022. Am J Med Genet A. 2007. PMID: 18000911

8

Cornelia de Lange syndrome (CdLS): prenatal and autopsy findings.

Chong K, Keating S, Hurst S, Summers A, Berger H, Seaward G, Martin N, Friedberg T, Chitayat D. Chong K, et al. Among authors: chitayat d. Prenat Diagn. 2009 May;29(5):489-94. doi: 10.1002/pd.2228. Prenat Diagn. 2009. PMID: 19242925

9

Fetal ventriculomegaly secondary to isolated large choroid plexus cysts: prenatal findings and postnatal outcome.

Fong K, Chong K, Toi A, Uster T, Blaser S, Chitayat D. Fong K, et al. Among authors: chitayat d. Prenat Diagn. 2011 Apr;31(4):395-400. doi: 10.1002/pd.2703. Epub 2011 Feb 16. Prenat Diagn. 2011. PMID: 21328578

10

Euchromatic 9q13-q21 duplication variants are tandem segmental amplifications of sequence reciprocal to 9q13-q21 deletions.

Joseph-George AM, He Y, Marshall CR, Wong RC, MacDonald JR, Fahey CA, Chitayat D, Chun K, Ryan G, Summers AM, Winsor EJ, Scherer SW. Joseph-George AM, et al. Among authors: chitayat d. J Med Genet. 2011 May;48(5):317-22. doi: 10.1136/jmg.2010.085662. Epub 2011 Mar 23. J Med Genet. 2011. PMID: 21429932

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