Van Dyke DL - Search Results

1

Diagnostic testing: a cost analysis for Prader-Willi and Angelman syndromes.

Monaghan KG, Van Dyke DL, Feldman G, Wiktor A, Weiss L. Monaghan KG, et al. Among authors: van dyke dl. Am J Hum Genet. 1997 Jan;60(1):244-7. Am J Hum Genet. 1997. PMID: 8981972 Free PMC article. No abstract available.

2

Diagnostic testing for Prader-Willi syndrome and Angelman syndrome: a cost comparison.

Monaghan KG, Wiktor A, Van Dyke DL. Monaghan KG, et al. Among authors: van dyke dl. Genet Med. 2002 Nov-Dec;4(6):448-50. doi: 10.1097/00125817-200211000-00009. Genet Med. 2002. PMID: 12509717 Free article.

3

Prader-Willi-like syndrome in a patient with an Xq23q25 duplication.

Monaghan KG, Van Dyke DL, Feldman GL. Monaghan KG, et al. Among authors: van dyke dl. Am J Med Genet. 1998 Nov 16;80(3):227-31. doi: 10.1002/(sici)1096-8628(19981116)80:3<227::aid-ajmg10>3.0.co;2-q. Am J Med Genet. 1998. PMID: 9843044

4

Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.

Zenger-Hain JL, Van Dyke DL, Wiktor A, Walker H, Feldman GL. Zenger-Hain JL, et al. Among authors: van dyke dl. Am J Med Genet. 1993 Dec 1;47(8):1198-201. doi: 10.1002/ajmg.1320470814. Am J Med Genet. 1993. PMID: 8291556

5

Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NF1).

Wiktor A, Van Dyke DL, Weiss L. Wiktor A, et al. Among authors: van dyke dl. Am J Med Genet. 1993 Jan 1;45(1):22-4. doi: 10.1002/ajmg.1320450108. Am J Med Genet. 1993. PMID: 8418653

6

Combined cytogenetic testing and fluorescence in situ hybridization analysis in the study of chronic lymphocytic leukemia and multiple myeloma.

Wiktor A, Van Dyke DL. Wiktor A, et al. Among authors: van dyke dl. Cancer Genet Cytogenet. 2004 Aug;153(1):73-6. doi: 10.1016/j.cancergencyto.2004.03.006. Cancer Genet Cytogenet. 2004. PMID: 15325099

7

FISH analysis helps identify low-level mosaicism in Ullrich-Turner syndrome patients.

Wiktor A, Van Dyke DL. Wiktor A, et al. Among authors: van dyke dl. Genet Med. 2004 May-Jun;6(3):132-5. doi: 10.1097/01.gim.0000127270.49902.56. Genet Med. 2004. PMID: 15354330

8

Detection of low level sex chromosome mosaicism in Ullrich-Turner syndrome patients.

Wiktor AE, Van Dyke DL. Wiktor AE, et al. Among authors: van dyke dl. Am J Med Genet A. 2005 Oct 15;138A(3):259-61. doi: 10.1002/ajmg.a.30954. Am J Med Genet A. 2005. PMID: 16158437

9

10p duplication characterized by fluorescence in situ hybridization.

Wiktor A, Feldman GL, Kratkoczki P, Ditmars DM Jr, Van Dyke DL. Wiktor A, et al. Among authors: van dyke dl. Am J Med Genet. 1994 Sep 1;52(3):315-8. doi: 10.1002/ajmg.1320520312. Am J Med Genet. 1994. PMID: 7528972

10

Molecular characterization of de novo secondary trisomy 13.

Shaffer LG, McCaskill C, Han JY, Choo KH, Cutillo DM, Donnenfeld AE, Weiss L, Van Dyke DL. Shaffer LG, et al. Among authors: van dyke dl. Am J Hum Genet. 1994 Nov;55(5):968-74. Am J Hum Genet. 1994. PMID: 7977360 Free PMC article.

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