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

por Mu, Y, Van Dyke, D L, Weiss, L, Olgac, S
Publicado 1984

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

por Flejter, W L, Van Dyke, D L, Weiss, L
Publicado 1984

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

por Babu, V R, Van Dyke, D L, Jackson, C E
Publicado 1984

The origin and behavior of two isodicentric bisatellited chromosomes.

por Van Dyke, D L, Weiss, L, Logan, M, Pai, G S
Publicado 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...

por Czarnecki, P M, Van Dyke, D L, Vats, S, Feldman, G L
Publicado 1998

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

por Van Dyke, D L, Weiss, L, Roberson, J R, Babu, V R
Publicado 1983

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

por Gaba, A R, Anderson, G J, VanDyke, D L, Chason, J L
Publicado 1982

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

por White, W M, Willard, H F, Van Dyke, D L, Wolff, D J
Publicado 1998

Chromosome polymorphism and twin zygosity.

por Van Dyke, D L, Palmer, C G, Nance, W E, Yu, P L
Publicado 1977

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

por Monaghan, K G, Van Dyke, D L, Feldman, G, Wiktor, A, Weiss, L
Publicado 1997

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

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

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

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

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

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

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

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

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

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

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

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

Molecular characterization of de novo secondary trisomy 13.

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

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

por 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
Publicado 1993

A practical metaphase marker of the inactive X chromosome.

por 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
Publicado 1986

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

por 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
Publicado 2006