Chen XN - Search Results

1

Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.

Cargile CB, Goh DL, Goodman BK, Chen XN, Korenberg JR, Semenza GL, Thomas GH. Cargile CB, et al. Among authors: chen xn. Am J Med Genet. 2002 Apr 22;109(2):133-8. doi: 10.1002/ajmg.10323. Am J Med Genet. 2002. PMID: 11977162

2

Deletion of chromosome 21 disturbs human brain morphogenesis.

Yao G, Chen XN, Flores-Sarnat L, Barlow GM, Palka G, Moeschler JB, McGillivray B, Morse RP, Korenberg JR. Yao G, et al. Among authors: chen xn. Genet Med. 2006 Jan;8(1):1-7. doi: 10.1097/01.gim.0000195892.60506.3f. Genet Med. 2006. PMID: 16418593 Free article.

3

Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12).

Cargile CB, McIntosh I, Clough MV, Rutberg J, Yaghmai R, Goodman BK, Chen XN, Korenberg JR, Thomas GH, Geraghty MT. Cargile CB, et al. Among authors: chen xn. Am J Med Genet. 2000 Jun 19;92(5):328-35. doi: 10.1002/1096-8628(20000619)92:5<328::aid-ajmg7>3.0.co;2-p. Am J Med Genet. 2000. PMID: 10861662

4

BAC resource for molecular cytogenetics.

Chen XN, Korenberg JR. Chen XN, et al. Methods Mol Biol. 2002;204:391-403. doi: 10.1385/1-59259-300-3:391. Methods Mol Biol. 2002. PMID: 12397812 No abstract available.

5

Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23.

Hirota H, Matsuoka R, Chen XN, Salandanan LS, Lincoln A, Rose FE, Sunahara M, Osawa M, Bellugi U, Korenberg JR. Hirota H, et al. Among authors: chen xn. Genet Med. 2003 Jul-Aug;5(4):311-21. doi: 10.1097/01.GIM.0000076975.10224.67. Genet Med. 2003. PMID: 12865760

6

BAC mapping using fluorescence in situ hybridization.

Chen XN, Korenberg JR. Chen XN, et al. Methods Mol Biol. 2004;255:131-41. doi: 10.1385/1-59259-752-1:131. Methods Mol Biol. 2004. PMID: 15020820 No abstract available.

7

Localization of human CREBBP (CREB binding protein) to 16p13.3 by fluorescence in situ hybridization.

Chen XN, Korenberg JR. Chen XN, et al. Cytogenet Cell Genet. 1995;71(1):56-7. doi: 10.1159/000134062. Cytogenet Cell Genet. 1995. PMID: 7606928

8

Human cDNA mapping using a high-resolution R-banding technique and fluorescence in situ hybridization.

Korenberg JR, Chen XN. Korenberg JR, et al. Among authors: chen xn. Cytogenet Cell Genet. 1995;69(3-4):196-200. doi: 10.1159/000133962. Cytogenet Cell Genet. 1995. PMID: 7698011

9

Localization of the human RGR opsin gene to chromosome 10q23.

Chen XN, Korenberg JR, Jiang M, Shen D, Fong HK. Chen XN, et al. Hum Genet. 1996 Jun;97(6):720-2. doi: 10.1007/BF02346179. Hum Genet. 1996. PMID: 8641686

10

Assignment of the GOV (Glioblastoma overexpressed) gene to human chromosome band 19p13.2 by fluorescence in situ hybridization.

Chen XN, Shi ZY, Korenberg JR, Sehgal A. Chen XN, et al. Cytogenet Cell Genet. 1998;83(3-4):230-1. doi: 10.1159/000015187. Cytogenet Cell Genet. 1998. PMID: 10072586 No abstract available.

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