Raca G - Search Results

1

Clinical and molecular characterization of overlapping interstitial Xp21-p22 duplications in two unrelated individuals.

Thorson L, Bryke C, Rice G, Artzer A, Schilz C, Israel J, Huber S, Laffin J, Raca G. Thorson L, et al. Among authors: raca g. Am J Med Genet A. 2010 Apr;152A(4):904-15. doi: 10.1002/ajmg.a.33340. Am J Med Genet A. 2010. PMID: 20358600

2

Phenotype of FOXP2 haploinsufficiency in a mother and son.

Rice GM, Raca G, Jakielski KJ, Laffin JJ, Iyama-Kurtycz CM, Hartley SL, Sprague RE, Heintzelman AT, Shriberg LD. Rice GM, et al. Among authors: raca g. Am J Med Genet A. 2012 Jan;158A(1):174-81. doi: 10.1002/ajmg.a.34354. Epub 2011 Nov 21. Am J Med Genet A. 2012. PMID: 22106036 Free PMC article.

3

Array-based comparative genomic hybridization (aCGH) in the genetic evaluation of stillbirth.

Raca G, Artzer A, Thorson L, Huber S, Modaff P, Laffin J, Pauli RM. Raca G, et al. Am J Med Genet A. 2009 Nov;149A(11):2437-43. doi: 10.1002/ajmg.a.33083. Am J Med Genet A. 2009. PMID: 19876905

4

Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization.

Laffin JJ, Raca G, Jackson CA, Strand EA, Jakielski KJ, Shriberg LD. Laffin JJ, et al. Among authors: raca g. Genet Med. 2012 Nov;14(11):928-36. doi: 10.1038/gim.2012.72. Epub 2012 Jul 5. Genet Med. 2012. PMID: 22766611 Free PMC article.

5

Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.

Raca G, Baas BS, Kirmani S, Laffin JJ, Jackson CA, Strand EA, Jakielski KJ, Shriberg LD. Raca G, et al. Eur J Hum Genet. 2013 Apr;21(4):455-9. doi: 10.1038/ejhg.2012.165. Epub 2012 Aug 22. Eur J Hum Genet. 2013. PMID: 22909774 Free PMC article.

6

The advantage of using SNP array in clinical testing for hematological malignancies--a comparative study of three genetic testing methods.

Xu X, Johnson EB, Leverton L, Arthur A, Watson Q, Chang FL, Raca G, Laffin JJ. Xu X, et al. Among authors: raca g. Cancer Genet. 2013 Sep-Oct;206(9-10):317-26. doi: 10.1016/j.cancergen.2013.09.001. Epub 2013 Oct 24. Cancer Genet. 2013. PMID: 24269304

7

MECP2 duplication: possible cause of severe phenotype in females.

Scott Schwoerer J, Laffin J, Haun J, Raca G, Friez MJ, Giampietro PF. Scott Schwoerer J, et al. Among authors: raca g. Am J Med Genet A. 2014 Apr;164A(4):1029-34. doi: 10.1002/ajmg.a.36380. Epub 2014 Jan 23. Am J Med Genet A. 2014. PMID: 24458799

8

Mild clinical presentation in a child with prenatally diagnosed 45,X/47,XX,+18 mosaicism.

Tyler CT, Rice GM, Grady M, Raca G. Tyler CT, et al. Among authors: raca g. Am J Med Genet A. 2009 Nov;149A(11):2588-92. doi: 10.1002/ajmg.a.33084. Am J Med Genet A. 2009. PMID: 19876897 No abstract available.

9

Chromosomal abnormalities in 2 cases of testicular failure.

Chen X, Raca G, Laffin J, Babaian KN, Williams DH. Chen X, et al. Among authors: raca g. J Androl. 2011 May-Jun;32(3):226-31. doi: 10.2164/jandrol.110.010280. Epub 2010 Oct 21. J Androl. 2011. PMID: 20966427

10

DNA methylation assay for X-chromosome inactivation in female human iPS cells.

Kiedrowski LA, Raca G, Laffin JJ, Nisler BS, Leonhard K, McIntire E, Mongomery KD. Kiedrowski LA, et al. Among authors: raca g. Stem Cell Rev Rep. 2011 Nov;7(4):969-75. doi: 10.1007/s12015-011-9238-6. Stem Cell Rev Rep. 2011. PMID: 21373884

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