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Published in Nature genetics (01.04.1996)
Published in Nature genetics (01.04.1996)
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Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency
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Published in Clinical genetics (01.05.2000)
Published in Clinical genetics (01.05.2000)
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Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT)
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
Published in Prenatal diagnosis (01.07.1999)
Published in Prenatal diagnosis (01.07.1999)
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Correction of the spontaneous and DEB-induced chromosomal aberrations in Fanconi anemia cells of the FA(C) complementation group by the FACC gene
STAVROPOULOS, D. J, SOOD, S, TOMKINS, D. J, BUCHWALD, M
Published in Cytogenetic and genome research (01.01.1996)
Published in Cytogenetic and genome research (01.01.1996)
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Conference Proceeding
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Mapping of a Single Locus Capable of Complementing the Defective Heterochromatin Phenotype of Roberts Syndrome Cells
McDaniel, Lisa D., Tomkins, Darrell J., Stanbridge, Eric J., Somerville, Martin J., Friedberg, Errol C., Schultz, Roger A.
Published in American journal of human genetics (01.07.2005)
Published in American journal of human genetics (01.07.2005)
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Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism
Nowaczyk, M J, Ramsay, J A, Mohide, P, Tomkins, D J
Published in American journal of medical genetics (26.05.1998)
Published in American journal of medical genetics (26.05.1998)
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Journal Article
De novo deletion 12q: report of a patient with 12q24.31q24.33 deletion
Sathya, P, Tomkins, D J, Freeman, V, Paes, B, Nowaczyk, M J
Published in American journal of medical genetics (21.05.1999)
Published in American journal of medical genetics (21.05.1999)
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