Huang XL - Search Results

1

Modification of CMT1 phenotypes by the independent coexisting neurogenetic disorders, McArdle disease and chromosome 5p trisomy.

Thomas FP, Geller TJ, Hahn AF, Gutmann L, Huang XL, Wu H, Wyandt HE, Lebo RV. Thomas FP, et al. Among authors: huang xl. Ann N Y Acad Sci. 1999 Sep 14;883:472-6. Ann N Y Acad Sci. 1999. PMID: 10586277 No abstract available.

2

Modification of CMT1 Phenotypes by the Independent Coexisting Neurogenetic Disorders, McArdle Disease and Chromosome 5p Trisomy.

Thomas FP, Geller TJ, Hahn AF, Gutmann L, Huang XL, Wu H, Wyandt HE, Lebo RV. Thomas FP, et al. Among authors: huang xl. Ann N Y Acad Sci. 1999 Oct;883(1):472-476. doi: 10.1111/j.1749-6632.1999.tb08614.x. Ann N Y Acad Sci. 1999. PMID: 29086973 No abstract available.

3

Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization.

Mark HF, Wyandt H, Huang XL, Milunsky JM. Mark HF, et al. Among authors: huang xl. Clin Genet. 2005 Aug;68(2):146-51. doi: 10.1111/j.1399-0004.2005.00466.x. Clin Genet. 2005. PMID: 15996211

4

Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant.

Milunsky JM, Wyandt HE, Huang XL, Kang XZ, Elias ER, Milunsky A. Milunsky JM, et al. Among authors: huang xl. Am J Med Genet. 1996 Jan 22;61(3):269-73. doi: 10.1002/(SICI)1096-8628(19960122)61:3<269::AID-AJMG12>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8741873

5

Schizophrenia susceptibility gene locus at Xp22.3.

Milunsky J, Huang XL, Wyandt HE, Milunsky A. Milunsky J, et al. Among authors: huang xl. Clin Genet. 1999 Jun;55(6):455-60. doi: 10.1034/j.1399-0004.1999.550610.x. Clin Genet. 1999. PMID: 10450863

6

Correlation of abnormal rapid FISH and chromosome results from amniocytes for prenatal diagnosis.

Wyandt HE, Tonk VS, Huang XL, Evans AT, Milunsky JM, Milunsky A. Wyandt HE, et al. Among authors: huang xl. Fetal Diagn Ther. 2006;21(2):235-40. doi: 10.1159/000089310. Fetal Diagn Ther. 2006. PMID: 16491010 Clinical Trial.

7

Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.

Wyandt HE, Shim SH, Mark HF, Huang XL, Milunsky JM. Wyandt HE, et al. Among authors: huang xl. Exp Mol Pathol. 2006 Jun;80(3):262-6. doi: 10.1016/j.yexmp.2005.12.008. Epub 2006 Mar 6. Exp Mol Pathol. 2006. PMID: 16516886

8

Symmetric replication of an unstable isodicentric Xq chromosome derived from isolocal maternal sister chromatid recombination.

Lebo RV, Milunsky J, Higgins AW, Loose B, Huang XL, Wyandt HE. Lebo RV, et al. Among authors: huang xl. Am J Med Genet. 1999 Aug 27;85(5):429-37. Am J Med Genet. 1999. PMID: 10405438

9

Disease associated balanced chromosome rearrangements (DBCR): report of two new cases.

Tonk VS, Wyandt HE, Huang X, Patel N, Morgan DL, Kukolich M, Lockhart LH, Velagaleti GV. Tonk VS, et al. Ann Genet. 2003 Jan-Mar;46(1):37-43. doi: 10.1016/s0003-3995(03)00005-4. Ann Genet. 2003. PMID: 12818528

10

FISH Variants with D15Z1.

Shim SH, Pan A, Huang XL, Tonk VS, Varma SK, Milunsky JM, Wyandt HE. Shim SH, et al. Among authors: huang xl. J Assoc Genet Technol. 2003;29(4):146-151. J Assoc Genet Technol. 2003. PMID: 15213412

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