Van Dyke DL - Search Results

1

Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy.

Berend SA, Feldman GL, McCaskill C, Czarnecki P, Van Dyke DL, Shaffer LG. Berend SA, et al. Among authors: van dyke dl. Am J Med Genet. 1999 Jan 29;82(3):275-81. doi: 10.1002/(sici)1096-8628(19990129)82:3<275::aid-ajmg15>3.0.co;2-2. Am J Med Genet. 1999. PMID: 10215554

2

Replication banding and molecular studies of a mosaic, unbalanced dic(X;15)(Xpter-->Xq26.1::15p11-->15qter).

Scheuerle A, Zenger-Hain JL, Van Dyke DL, Ledbetter DH, Greenberg F, Shaffer LG. Scheuerle A, et al. Among authors: van dyke dl. Am J Med Genet. 1995 May 8;56(4):403-8. doi: 10.1002/ajmg.1320560411. Am J Med Genet. 1995. PMID: 7604850

3

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.

4

Inverted duplication of 8p: ten new patients and review of the literature.

Feldman GL, Weiss L, Phelan MC, Schroer RJ, Van Dyke DL. Feldman GL, et al. Among authors: van dyke dl. Am J Med Genet. 1993 Sep 15;47(4):482-6. doi: 10.1002/ajmg.1320470410. Am J Med Genet. 1993. PMID: 8256810 Review.

5

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

6

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

7

Mosaicism for trisomy 12: four cases with varying outcomes.

Bischoff FZ, Zenger-Hain J, Moses D, Van Dyke DL, Shaffer LG. Bischoff FZ, et al. Among authors: van dyke dl. Prenat Diagn. 1995 Nov;15(11):1017-26. doi: 10.1002/pd.1970151106. Prenat Diagn. 1995. PMID: 8606880

8

Cytogenetic and clinical findings in a patient with a deletion of 16q23.1: first report of bilateral cataracts and a 16q deletion.

Monaghan KG, Van Dyke DL, Wiktor A, Feldman GL. Monaghan KG, et al. Among authors: van dyke dl. Am J Med Genet. 1997 Dec 12;73(2):180-3. doi: 10.1002/(sici)1096-8628(1997)73:2<180::aid-ajmg13>3.0.co;2-q. Am J Med Genet. 1997. PMID: 9409869 Review.

9

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

10

Child with velocardiofacial syndrome and del (4)(q34.2): another critical region associated with a velocardiofacial syndrome-like phenotype.

Tsai CH, Van Dyke DL, Feldman GL. Tsai CH, et al. Among authors: van dyke dl. Am J Med Genet. 1999 Feb 12;82(4):336-9. Am J Med Genet. 1999. PMID: 10051168 Review.

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