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

著者: Mu, Y, Van Dyke, D L, Weiss, L, Olgac, S
出版事項 1984

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

著者: Flejter, W L, Van Dyke, D L, Weiss, L
出版事項 1984

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

著者: Babu, V R, Van Dyke, D L, Jackson, C E
出版事項 1984

The origin and behavior of two isodicentric bisatellited chromosomes.

著者: Van Dyke, D L, Weiss, L, Logan, M, Pai, G S
出版事項 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...

著者: Czarnecki, P M, Van Dyke, D L, Vats, S, Feldman, G L
出版事項 1998

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

著者: Van Dyke, D L, Weiss, L, Roberson, J R, Babu, V R
出版事項 1983

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

著者: Gaba, A R, Anderson, G J, VanDyke, D L, Chason, J L
出版事項 1982

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

著者: White, W M, Willard, H F, Van Dyke, D L, Wolff, D J
出版事項 1998

Chromosome polymorphism and twin zygosity.

著者: Van Dyke, D L, Palmer, C G, Nance, W E, Yu, P L
出版事項 1977

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

著者: Monaghan, K G, Van Dyke, D L, Feldman, G, Wiktor, A, Weiss, L
出版事項 1997

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

著者: Wolff, D. J., Miller, A. P., Van Dyke, D. L., Schwartz, S., Willard, H. F.
出版事項 1996

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

著者: Worsham, M J, Wolman, S R, Carey, T E, Zarbo, R J, Benninger, M S, Van Dyke, D L
出版事項 1999

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

著者: Bodrug, S E, Roberson, J R, Weiss, L, Ray, P N, Worton, R G, Van Dyke, D L
出版事項 1990

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

著者: Caramazza, D, Begna, K H, Gangat, N, Vaidya, R, Siragusa, S, Van Dyke, D L, Hanson, C, Pardanani, A, Tefferi, A
出版事項 2011

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

著者: Nowinski, G P, Van Dyke, D L, Tilley, B C, Jacobsen, G, Babu, V R, Worsham, M J, Wilson, G N, Weiss, L
出版事項 1990

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

著者: Worsham, M J, Miller, D A, Devries, J M, Mitchell, A R, Babu, V R, Surli, V, Weiss, L, Van Dyke, D L
出版事項 1989

Molecular characterization of de novo secondary trisomy 13.

著者: Shaffer, L. G., McCaskill, C., Han, J. Y., Choo, K. H., Cutillo, D. M., Donnenfeld, A. E., Weiss, L., Van Dyke, D. L.
出版事項 1994

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

著者: 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
出版事項 1993

A practical metaphase marker of the inactive X chromosome.

著者: 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
出版事項 1986

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

著者: 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
出版事項 2006