Wyandt HE - Search Results

1

Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.

Prabhakara K, Wyandt HE, Huang XL, Prasad KS, Ramadevi AR. Prabhakara K, et al. Among authors: wyandt he. Ann Genet. 2004 Jul-Sep;47(3):297-303. doi: 10.1016/j.anngen.2004.03.007. Ann Genet. 2004. PMID: 15337476

2

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. Among authors: wyandt he. Ann Genet. 2003 Jan-Mar;46(1):37-43. doi: 10.1016/s0003-3995(03)00005-4. Ann Genet. 2003. PMID: 12818528

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. 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: wyandt he. 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

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. Fetal Diagn Ther. 2006;21(2):235-40. doi: 10.1159/000089310. Fetal Diagn Ther. 2006. PMID: 16491010 Clinical Trial.

6

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. 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

7

Schizophrenia susceptibility gene locus at Xp22.3.

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

Patient 1 was previously reported by us (Wyandt HE, Bugeau-Michaud L, Skare JC, Milunsky A. Partial duplication of Xp: a case report and review of previously reported cases. ...

Patient 1 was previously reported by us (Wyandt HE, Bugeau-Michaud L, Skare JC, Milunsky A. Partial duplication of Xp: a case …

8

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: wyandt he. Ann N Y Acad Sci. 1999 Sep 14;883:472-6. Ann N Y Acad Sci. 1999. PMID: 10586277 No abstract available.

9

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: wyandt he. Am J Med Genet. 1999 Aug 27;85(5):429-37. Am J Med Genet. 1999. PMID: 10405438

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: wyandt he. J Assoc Genet Technol. 2003;29(4):146-151. J Assoc Genet Technol. 2003. PMID: 15213412

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