VanDyke DL - Search Results

1

Alobar holoprosencephaly and otocephaly in a female infant with a normal karyotype and placental villitis.

Gaba AR, Anderson GJ, VanDyke DL, Chason JL. Gaba AR, et al. Among authors: vandyke dl. J Med Genet. 1982 Feb;19(1):78. doi: 10.1136/jmg.19.1.78. J Med Genet. 1982. PMID: 7069754 Free PMC article. No abstract available.

2

Dysgenetic male pseudohermaphroditism in a 45,X/46,X,del(Y)(q11.1) mosaic infant.

Gaba AR, Van Dyke DL, Weiss L. Gaba AR, et al. Am J Med Genet. 1987 Mar;26(3):545-9. doi: 10.1002/ajmg.1320260306. Am J Med Genet. 1987. PMID: 3565468

3

De novo direct tandem duplication of the proximal long arm of chromosome 2: 46,XX,dir dup(2)(q11 X 2q14 X 2).

Mu Y, Van Dyke DL, Weiss L, Olgac S. Mu Y, et al. J Med Genet. 1984 Feb;21(1):57-8. doi: 10.1136/jmg.21.1.57. J Med Genet. 1984. PMID: 6694186 Free PMC article.

4

Malformation syndrome of duplication 12q24.1 leads to qter.

Melnyk AR, Weiss L, Van Dyke DL, Jarvi P. Melnyk AR, et al. Am J Med Genet. 1981;10(4):357-65. doi: 10.1002/ajmg.1320100408. Am J Med Genet. 1981. PMID: 7332029

5

Secondary trisomy or mosaic "tetrasomy" 8p.

Robinow M, Haney N, Chen H, Sorauf T, Van Dyke DL, Babu VR, Powell S, Maliszewski W, Guerin S, Landers JW. Robinow M, et al. Am J Med Genet. 1989 Mar;32(3):320-4. doi: 10.1002/ajmg.1320320309. Am J Med Genet. 1989. PMID: 2729351

6

Chromosome 20 deletion in multiple endocrine neoplasia type 2: expanded double-blind studies.

Babu VR, Van Dyke DL, Flejter WL, Jackson CE. Babu VR, et al. Am J Med Genet. 1987 Jul;27(3):739-48. doi: 10.1002/ajmg.1320270336. Am J Med Genet. 1987. PMID: 2888311

7

Duplication 3p21----3pter and cyclopia.

Kurtzman DN, Van Dyke DL, Rich CA, Weiss L. Kurtzman DN, et al. Am J Med Genet. 1987 May;27(1):33-7. doi: 10.1002/ajmg.1320270105. Am J Med Genet. 1987. PMID: 3605204 Free article.

8

Interstitial deletion of chromosome 10, del(10) (q11.2q22.1) in a boy with developmental delay and multiple congenital anomalies.

Zenger-Hain JL, Roberson J, Van Dyke DL, Weiss L. Zenger-Hain JL, et al. Am J Med Genet. 1993 Jun 1;46(4):438-40. doi: 10.1002/ajmg.1320460418. Am J Med Genet. 1993. PMID: 7689299

9

Mother and son with deletion of 3p25-pter.

Tazelaar J, Roberson J, Van Dyke DL, Babu VR, Weiss L. Tazelaar J, et al. Am J Med Genet. 1991 May 1;39(2):130-2. doi: 10.1002/ajmg.1320390203. Am J Med Genet. 1991. PMID: 2063913

10

10p duplication characterized by fluorescence in situ hybridization.

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

222 results

Search Page

Filters