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

ανά Mu, Y, Van Dyke, D L, Weiss, L, Olgac, S
Έκδοση 1984

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

ανά Flejter, W L, Van Dyke, D L, Weiss, L
Έκδοση 1984

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

ανά Babu, V R, Van Dyke, D L, Jackson, C E
Έκδοση 1984

The origin and behavior of two isodicentric bisatellited chromosomes.

ανά Van Dyke, D L, Weiss, L, Logan, M, Pai, G S
Έκδοση 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...

ανά Czarnecki, P M, Van Dyke, D L, Vats, S, Feldman, G L
Έκδοση 1998

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

ανά Van Dyke, D L, Weiss, L, Roberson, J R, Babu, V R
Έκδοση 1983

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

ανά Gaba, A R, Anderson, G J, VanDyke, D L, Chason, J L
Έκδοση 1982

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

ανά White, W M, Willard, H F, Van Dyke, D L, Wolff, D J
Έκδοση 1998

Chromosome polymorphism and twin zygosity.

ανά Van Dyke, D L, Palmer, C G, Nance, W E, Yu, P L
Έκδοση 1977

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

ανά Monaghan, K G, Van Dyke, D L, Feldman, G, Wiktor, A, Weiss, L
Έκδοση 1997

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

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

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

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

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

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

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

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

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

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

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

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

Molecular characterization of de novo secondary trisomy 13.

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

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

ανά 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
Έκδοση 1993

A practical metaphase marker of the inactive X chromosome.

ανά 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
Έκδοση 1986

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

ανά 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
Έκδοση 2006