Van Dyke DL - Search Results

1

Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay.

Asamoah A, Decker AB, Wiktor A, Van Dyke DL. Asamoah A, et al. Among authors: van dyke dl. Am J Med Genet A. 2003 Apr 1;118A(1):82-5. doi: 10.1002/ajmg.a.10929. Am J Med Genet A. 2003. PMID: 12605448

2

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

3

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

4

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

5

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.

6

Monosomy 21 in hematologic diseases.

Van Dyke DL, Wiktor A. Van Dyke DL, et al. Cancer Genet Cytogenet. 2003 Apr 15;142(2):137-41. doi: 10.1016/s0165-4608(02)00796-3. Cancer Genet Cytogenet. 2003. PMID: 12699891

7

Translocation (8;14)(q24;q32) as the sole cytogenetic abnormality in B-cell prolymphocytic leukemia.

Kuriakose P, Perveen N, Maeda K, Wiktor A, Van Dyke DL. Kuriakose P, et al. Among authors: van dyke dl. Cancer Genet Cytogenet. 2004 Apr 15;150(2):156-8. doi: 10.1016/j.cancergencyto.2003.09.009. Cancer Genet Cytogenet. 2004. PMID: 15066324

8

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

9

Ullrich-Turner syndrome with a small ring X chromosome and presence of mental retardation.

Van Dyke DL, Wiktor A, Palmer CG, Miller DA, Witt M, Babu VR, Worsham MJ, Roberson JR, Weiss L. Van Dyke DL, et al. Am J Med Genet. 1992 Aug 1;43(6):996-1005. doi: 10.1002/ajmg.1320430617. Am J Med Genet. 1992. PMID: 1415351 Review.

10

X-inactivation pattern in an Ullrich-Turner syndrome patient with a small ring X and normal intelligence.

Zenger-Hain JL, Wiktor A, Goldman J, Van Dyke DL, Weiss L. Zenger-Hain JL, et al. Among authors: van dyke dl. Am J Med Genet. 1993 Sep 15;47(4):490-3. doi: 10.1002/ajmg.1320470412. Am J Med Genet. 1993. PMID: 8256812

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