Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia von Chen, Ming, Tomkins, Darrell J, Auerbach, Wojtek, McKerlie, Colin, Youssoufian, Hagop, Liu, Lili, Gan, Olga, Carreau, Madeleine, Auerbach, Anna, Groves, Tim, Guidos, Cynthia J, Freedman, Melvin H, Cross, Jay, Percy, Dean H, Dick, John E, Joyner, Alexandra L, Buchwald, Manuel

Volltext

Case-control study of congenital anomalies in children of cancer patients von Dodds, L, Marrett, L D, Tomkins, D J, Green, B, Sherman, G

Volltext

Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency von Nowaczyk, Małgorzata Jm, Huggins, Marlene J, Tomkins, Darrell J, Rossi, Elena, Ramsay, Jennifer A, Woulfe, John, Scherer, Stephen W, Belloni, Elena

Volltext

Risk of congenital anomalies in children of parents occupationally exposed to low level ionising radiation von Green, L M, Dodds, L, Miller, A B, Tomkins, D J, Li, J, Escobar, M

Volltext

Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT) von Winsor, Elizabeth J. T., Tomkins, Darrell J., Kalousek, Dagmar, Farrell, Sandra, Wyatt, Philip, Fan, Yao-Shan, Carter, Ronald, Wang, Hungshu, Dallaire, Louis, Eydoux, Patrice, Welch, J. Philip, Dawson, Angelika, Lin, Jim C. C., Singer, Joel, Johnson, JoAnn, Wilson, R. Douglas

Volltext

Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells von McDaniel, Lisa D., Tomkins, Darrell J., Stanbridge, Eric J., Somerville, Martin J., Friedberg, Errol C., Schultz, Roger A.

Volltext

A Study of Sister Chromatid Exchange and Somatic Cell Mutation in Hospital Workers Exposed to Ethylene Oxide von Tomkins, Darrell J., Haines, Ted, Lawrence, Murray, Rosa, Nadia

Volltext

Transformation of human cultured fibroblasts with plasmids carrying dominant selection markers and immortalizing potential von Chang, P.L., Gunby, J.L., Tomkins, D.J., Mak, I., Rosa, N.E., Mak, S.

Volltext

Prenatal diagnosis of holoprosencephaly (HPE) in a fetus with a recombinant (18)dup(18q)inv(18)(p11.31q11.2)mat von Leonard, Norma J., Tomkins, Darrell J., Demianczuk, Nestor

Volltext

Abnormalities in the cell-division cycle in Roberts syndrome fibroblasts: a cellular basis for the phenotypic characteristics? von Tomkins, D J, Sisken, J E

Volltext

Somatic cell hybridization of Roberts Syndrome and normal lymphoblasts resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypes von ALLINGHAM-HAWKINS, D. J, TOMKINS, D. J

Volltext

Diploid/tetraploid/t(1;6) mosaicism in a 17-year-old female with hypomelanosis of Ito, multiple congenital anomalies, and body asymmetry von Leonard, N.J., Tomkins, D.J.

Volltext

Unstable familial translocations: A t(11;22)mat inherited as a t(11;15) von Tomkins, D J

Volltext

Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism von Nowaczyk, Malgorzata J.M., Ramsay, Jennifer A., Mohide, Patrick, Tomkins, Darrell J.

Volltext

Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty von Tomkins, D J, Roux, A F, Waye, J, Freeman, V C, Cox, D W, Whelan, D T

Volltext

Randomised trial to assess safety and fetal outcome of early and midtrimester amniocentesis von Wilson, R, Johnson, J, Dansereau, J

Volltext

False-positive and false-negative cytogenetic findings on chorionic villus sampling von Tomkins, Darrell J., Vekemans, Michel J. J.

Volltext

Somatic cell hybridization of Roberts syndrome and normal human fibroblasts transfected with plasmids carrying dominant selection markers von GUNBY, J. L, TOMKINS, D. J, CHANG, P. L

Volltext

Heterogeneity in Roberts syndrome von Allingham-Hawkins, Diane J., Tomkins, Darrell J.

Volltext

Effect of sample holding, cryopreservation, and storage on the human lymphocyte cytogenetic test von Tomkins, Darrell J., Scheid, Elizabeth E.

Volltext