Wyandt H - Search Results

1

Clinical findings and linkage studies in familial tuberous sclerosis.

Short MP, Haines J, Jewell A, Bejjani B, Yang CH, Wyandt H, MacFarlane H, Andermann E, Kwiatkowski D, Amos J. Short MP, et al. Among authors: wyandt h. Ann N Y Acad Sci. 1991;615:380-1. doi: 10.1111/j.1749-6632.1991.tb37788.x. Ann N Y Acad Sci. 1991. PMID: 1645505 No abstract available.

2

46,XY/47,XYY male with the fragile X syndrome: cytogenetic and molecular studies.

Milunsky A, Huang X, Amos JA, Herskowitz J, Farrer LA, Wyandt HE. Milunsky A, et al. Among authors: wyandt he. Am J Med Genet. 1993 Mar 1;45(5):589-93. doi: 10.1002/ajmg.1320450514. Am J Med Genet. 1993. PMID: 8096117

3

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 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.

4

Familial supernumerary chromosome and malignancy.

Milunsky JM, Wyandt HE, Milunsky A. Milunsky JM, et al. Among authors: wyandt he. Cancer Genet Cytogenet. 1996 Jul 15;89(2):170-2. doi: 10.1016/0165-4608(96)00069-6. Cancer Genet Cytogenet. 1996. PMID: 8697427 Free article.

5

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

6

In situ hybridization applied to Waardenburg syndrome.

Wu BL, Milunsky A, Wyandt H, Hoth C, Baldwin C, Skare J. Wu BL, et al. Among authors: wyandt h. Cytogenet Cell Genet. 1993;63(1):29-32. doi: 10.1159/000133495. Cytogenet Cell Genet. 1993. PMID: 8449034

7

Localization of the gene for human heart fatty acid binding protein to chromosome 1p32-1p33.

Troxler RF, Offner GD, Jiang JW, Wu BL, Skare JC, Milunsky A, Wyandt HE. Troxler RF, et al. Among authors: wyandt he. Hum Genet. 1993 Dec;92(6):563-6. doi: 10.1007/BF00420939. Hum Genet. 1993. PMID: 8262516

8

Cytogenetic studies of an adrenal cortical carcinoma.

Marks JL, Wyandt HE, Beazley RM, Milunsky JM, Sheahan K, Milunsky A. Marks JL, et al. Among authors: wyandt he. Cancer Genet Cytogenet. 1992 Jul 1;61(1):96-8. doi: 10.1016/0165-4608(92)90377-k. Cancer Genet Cytogenet. 1992. PMID: 1638487

9

Tandem duplication/deletion in a maternally derived chromosome 9 supernumerary derivative resulting in 9p trisomy and partial 9q tetrasomy.

Wyandt HE, Lebo RV, Fenerci EY, Sadhu DN, Milunsky JM. Wyandt HE, et al. Am J Med Genet. 2000 Aug 14;93(4):305-12. Am J Med Genet. 2000. PMID: 10946358

10

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

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