Chong K - Search Results

1

Deletion of 15q11.2(BP1-BP2) region: further evidence for lack of phenotypic specificity in a pediatric population.

Hashemi B, Bassett A, Chitayat D, Chong K, Feldman M, Flanagan J, Goobie S, Kawamura A, Lowther C, Prasad C, Siu V, So J, Tung S, Speevak M, Stavropoulos DJ, Carter MT. Hashemi B, et al. Among authors: chong k. Am J Med Genet A. 2015 Sep;167A(9):2098-102. doi: 10.1002/ajmg.a.37134. Epub 2015 May 6. Am J Med Genet A. 2015. PMID: 25946043

2

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

Sermer D, Quercia N, Chong K, Chitayat D. Sermer D, et al. Among authors: chong k. 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

3

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. Among authors: chong k. 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

4

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. Prenat Diagn. 2009 May;29(5):489-94. doi: 10.1002/pd.2228. Prenat Diagn. 2009. PMID: 19242925

5

Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting.

Goobie S, Knijnenburg J, Fitzpatrick D, Sharkey FH, Lionel AC, Marshall CR, Azam T, Shago M, Chong K, Mendoza-Londono R, den Hollander NS, Ruivenkamp C, Maher E, Tanke HJ, Szuhai K, Wintle RF, Scherer SW. Goobie S, et al. Among authors: chong k. Cytogenet Genome Res. 2008;123(1-4):65-78. doi: 10.1159/000184693. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287140 Free PMC article.

6

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: chong k. Prenat Diagn. 2011 Apr;31(4):395-400. doi: 10.1002/pd.2703. Epub 2011 Feb 16. Prenat Diagn. 2011. PMID: 21328578

7

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: chong k. 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.

8

Diagnostic utility of microarray testing in pregnancy loss.

Rosenfeld JA, Tucker ME, Escobar LF, Neill NJ, Torchia BS, McDaniel LD, Schultz RA, Chong K, Chitayat D. Rosenfeld JA, et al. Among authors: chong k. Ultrasound Obstet Gynecol. 2015 Oct;46(4):478-86. doi: 10.1002/uog.14866. Epub 2015 Sep 1. Ultrasound Obstet Gynecol. 2015. PMID: 25846569 Free article.

9

Analysis of tissue from products of conception and perinatal losses using QF-PCR and microarray: A three-year retrospective study resulting in an efficient protocol.

Wou K, Hyun Y, Chitayat D, Vlasschaert M, Chong K, Wasim S, Keating S, Shannon P, Kolomietz E. Wou K, et al. Among authors: chong k. Eur J Med Genet. 2016 Aug;59(8):417-24. doi: 10.1016/j.ejmg.2016.05.011. Epub 2016 May 24. Eur J Med Genet. 2016. PMID: 27233578

10

Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell-Silver syndrome.

Cytrynbaum C, Chong K, Hannig V, Choufani S, Shuman C, Steele L, Morgan T, Scherer SW, Stavropoulos DJ, Basran RK, Weksberg R. Cytrynbaum C, et al. Among authors: chong k. Am J Med Genet A. 2016 Oct;170(10):2731-9. doi: 10.1002/ajmg.a.37819. Epub 2016 Jul 4. Am J Med Genet A. 2016. PMID: 27374371

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