Flejter, W L, McDaniel, L D, Johns, D, Friedberg, E C, Schultz, R A
Cultured cells from individuals afflicted with the genetically heterogeneous autosomal recessive disorder xeroderma pigmentosum (XP) exhibit sensitivity to UV radiation and defective nucleotide...
A gene involved in XY sex reversal is located on chromosome 9, distal to marker D9S1779.
Flejter, W L, Fergestad, J, Gorski, J, Varvill, T, Chandrasekharappa, S
The genetic mechanisms involved in sex differentiation are poorly understood, and progress in identification of the genes involved has been slow. The fortuitous finding of chromosomal rearrangements...
Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.
Zinn, A R, Tonk, V S, Chen, Z, Flejter, W L, Gardner, H A, Guerra, R, ...
Turner syndrome is the complex human phenotype associated with complete or partial monosomy X. Principle features of Turner syndrome include short stature, ovarian failure, and a variety of other...
A practical metaphase marker of the inactive X chromosome.
Van Dyke, D L, Flejter, W L, Worsham, M J, Roberson, J R, Higgins, J V, Herr, H M, ...
It is paradoxical that the inactivated X is the only chromosome that can be identified in the interphase nucleus, yet in metaphase, it is indistinguishable from its genetically active homolog unless...
Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center.
Flejter, W L, Van Dyke, D L, Weiss, L
Bends in mitotic metaphase chromosomes are not distributed randomly throughout the karyotype. The frequency of bends at centromeres is positively correlated with the relative length of the...
Flejter, W L, McDaniel, L D, Johns, D, Friedberg, E C, Schultz, R A
Cultured cells from individuals afflicted with the genetically heterogeneous autosomal recessive disorder xeroderma pigmentosum (XP) exhibit sensitivity to UV radiation and defective nucleotide...
A gene involved in XY sex reversal is located on chromosome 9, distal to marker D9S1779.
Flejter, W L, Fergestad, J, Gorski, J, Varvill, T, Chandrasekharappa, S
The genetic mechanisms involved in sex differentiation are poorly understood, and progress in identification of the genes involved has been slow. The fortuitous finding of chromosomal rearrangements...
Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.
Zinn, A R, Tonk, V S, Chen, Z, Flejter, W L, Gardner, H A, Guerra, R, ...
Turner syndrome is the complex human phenotype associated with complete or partial monosomy X. Principle features of Turner syndrome include short stature, ovarian failure, and a variety of other...
A practical metaphase marker of the inactive X chromosome.
Van Dyke, D L, Flejter, W L, Worsham, M J, Roberson, J R, Higgins, J V, Herr, H M, ...
It is paradoxical that the inactivated X is the only chromosome that can be identified in the interphase nucleus, yet in metaphase, it is indistinguishable from its genetically active homolog unless...
Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center.
Flejter, W L, Van Dyke, D L, Weiss, L
Bends in mitotic metaphase chromosomes are not distributed randomly throughout the karyotype. The frequency of bends at centromeres is positively correlated with the relative length of the...
Leana-Cox, J., Jenkins, L., Palmer, C. G., Plattner, R., Sheppard, L., Flejter, W. L., ...
Twenty-seven cases of inverted duplications of chromosome 15 (inv dup [15]) were investigated by FISH with two DNA probes specific for the Prader-Willi syndrome/Angelman syndrome (PWS/AS) region on...