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

per Mu, Y, Van Dyke, D L, Weiss, L, Olgac, S
Publicat 1984

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

per Flejter, W L, Van Dyke, D L, Weiss, L
Publicat 1984

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

per Babu, V R, Van Dyke, D L, Jackson, C E
Publicat 1984

The origin and behavior of two isodicentric bisatellited chromosomes.

per Van Dyke, D L, Weiss, L, Logan, M, Pai, G S
Publicat 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...

per Czarnecki, P M, Van Dyke, D L, Vats, S, Feldman, G L
Publicat 1998

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

per Van Dyke, D L, Weiss, L, Roberson, J R, Babu, V R
Publicat 1983

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

per Gaba, A R, Anderson, G J, VanDyke, D L, Chason, J L
Publicat 1982

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

per White, W M, Willard, H F, Van Dyke, D L, Wolff, D J
Publicat 1998

Chromosome polymorphism and twin zygosity.

per Van Dyke, D L, Palmer, C G, Nance, W E, Yu, P L
Publicat 1977

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

per Monaghan, K G, Van Dyke, D L, Feldman, G, Wiktor, A, Weiss, L
Publicat 1997

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

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

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

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

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

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

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

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

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

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

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

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

Molecular characterization of de novo secondary trisomy 13.

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

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

per 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
Publicat 1993

A practical metaphase marker of the inactive X chromosome.

per 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
Publicat 1986

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

per 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
Publicat 2006