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

od Mu, Y, Van Dyke, D L, Weiss, L, Olgac, S
Izdano 1984

Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center.

od Flejter, W L, Van Dyke, D L, Weiss, L
Izdano 1984

Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study.

od Babu, V R, Van Dyke, D L, Jackson, C E
Izdano 1984

The origin and behavior of two isodicentric bisatellited chromosomes.

od Van Dyke, D L, Weiss, L, Logan, M, Pai, G S
Izdano 1977

A mother with VCFS and unilateral dysplastic kidney and her fetus with multicystic dysplastic kidneys: additional evidence to support the association of renal malformations and VCF...

od Czarnecki, P M, Van Dyke, D L, Vats, S, Feldman, G L
Izdano 1998

The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age.

od Van Dyke, D L, Weiss, L, Roberson, J R, Babu, V R
Izdano 1983

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

od Gaba, A R, Anderson, G J, VanDyke, D L, Chason, J L
Izdano 1982

The spreading of X inactivation into autosomal material of an x;autosome translocation: evidence for a difference between autosomal and X-chromosomal DNA.

od White, W M, Willard, H F, Van Dyke, D L, Wolff, D J
Izdano 1998

Chromosome polymorphism and twin zygosity.

od Van Dyke, D L, Palmer, C G, Nance, W E, Yu, P L
Izdano 1977

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

od Monaghan, K G, Van Dyke, D L, Feldman, G, Wiktor, A, Weiss, L
Izdano 1997

Molecular definition of breakpoints associated with human Xq isochromosomes: implications for mechanisms of formation.

od Wolff, D. J., Miller, A. P., Van Dyke, D. L., Schwartz, S., Willard, H. F.
Izdano 1996

Chromosomal aberrations identified in culture of squamous carcinomas are confirmed by fluorescence in situ hybridisation.

od Worsham, M J, Wolman, S R, Carey, T E, Zarbo, R J, Benninger, M S, Van Dyke, D L
Izdano 1999

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

od Bodrug, S E, Roberson, J R, Weiss, L, Ray, P N, Worton, R G, Van Dyke, D L
Izdano 1990

Refined cytogenetic-risk categorization for overall and leukemia-free survival in primary myelofibrosis: a single center study of 433 patients

od Caramazza, D, Begna, K H, Gangat, N, Vaidya, R, Siragusa, S, Van Dyke, D L, Hanson, C, Pardanani, A, Tefferi, A
Izdano 2011

The frequency of aneuploidy in cultured lymphocytes is correlated with age and gender but not with reproductive history.

od Nowinski, G P, Van Dyke, D L, Tilley, B C, Jacobsen, G, Babu, V R, Worsham, M J, Wilson, G N, Weiss, L
Izdano 1990

A dicentric recombinant 9 derived from a paracentric inversion: phenotype, cytogenetics, and molecular analysis of centromeres.

od Worsham, M J, Miller, D A, Devries, J M, Mitchell, A R, Babu, V R, Surli, V, Weiss, L, Van Dyke, D L
Izdano 1989

Molecular characterization of de novo secondary trisomy 13.

od Shaffer, L. G., McCaskill, C., Han, J. Y., Choo, K. H., Cutillo, D. M., Donnenfeld, A. E., Weiss, L., Van Dyke, D. L.
Izdano 1994

Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypes.

od Migeon, B R, Luo, S, Stasiowski, B A, Jani, M, Axelman, J, Van Dyke, D L, Weiss, L, Jacobs, P A, Yang-Feng, T L, Wiley, J E
Izdano 1993

A practical metaphase marker of the inactive X chromosome.

od Van Dyke, D L, Flejter, W L, Worsham, M J, Roberson, J R, Higgins, J V, Herr, H M, Knuutila, S, Wang, N, Babu, V R, Weiss, L
Izdano 1986

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study

od Graf, M D, Christ, L, Mascarello, J T, Mowrey, P, Pettenati, M, Stetten, G, Storto, P, Surti, U, Van Dyke, D L, Vance, G H, Wolff, D, Schwartz, S
Izdano 2006