Your search returned 35 results.

Results
	21.	Development and characterization of immortalized fibroblastoid cell lines from an FA(C) mouse model. [electronic resource] by Tomkins, D J Care, M Carreau, M Buchwald, M Producer: 19980807 In: Mutation research vol. 408 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Canadian multicentre randomized clinical trial of chorion villus sampling and amniocentesis. Final report. [electronic resource] by Lippman, A Tomkins, D J Shime, J Hamerton, J L Producer: 19921014 In: Prenatal diagnosis vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Correction of the spontaneous and DEB-induced chromosomal aberrations in Fanconi anemia cells of the FA(C) complementation group by the FACC gene. [electronic resource] by Stavropoulos, D J Sood, S Tomkins, D J Buchwald, M Producer: 19970115 In: Cytogenetics and cell genetics vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Sister chromatid exchange response of human diploid fibroblasts and Chinese hamster ovary cells to dimethylnitrosamine and benzo(a)pyrene. [electronic resource] by Tomkins, D J Kwok, S E Douglas, G R Biggs, D Producer: 19820924 In: Environmental mutagenesis vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Multiple congenital anomalies in a fetus with 45,X/46,X,r(X)(p11.22q12) mosaicism. [electronic resource] by Nowaczyk, M J Ramsay, J A Mohide, P Tomkins, D J Producer: 19980707 In: American journal of medical genetics vol. 77 Availability: No items available. Save to lists Add to cart (remove)
	26.	De novo deletion 12q: report of a patient with 12q24.31q24.33 deletion. [electronic resource] by Sathya, P Tomkins, D J Freeman, V Paes, B Nowaczyk, M J Producer: 19990706 In: American journal of medical genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Two children with deletion of the long arm of chromosome 4 with breakpoint at band q33. [electronic resource] by Tomkins, D J Hunter, A G Uchida, I A Roberts, M H Producer: 19830407 In: Clinical genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Case-control study of congenital anomalies in children of cancer patients. [electronic resource] by Dodds, L Marrett, L D Tomkins, D J Green, B Sherman, G Producer: 19930909 In: BMJ (Clinical research ed.) vol. 307 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Risk of congenital anomalies in children of parents occupationally exposed to low level ionising radiation. [electronic resource] by Green, L M Dodds, L Miller, A B Tomkins, D J Li, J Escobar, M Producer: 19980113 In: Occupational and environmental medicine vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Transformation of human cultured fibroblasts with plasmids carrying dominant selection markers and immortalizing potential. [electronic resource] by Chang, P L Gunby, J L Tomkins, D J Mak, I Rosa, N E Mak, S Producer: 19861218 In: Experimental cell research vol. 167 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Maternal uniparental isodisomy of human chromosome 14 associated with a paternal t(13q14q) and precocious puberty. [electronic resource] by Tomkins, D J Roux, A F Waye, J Freeman, V C Cox, D W Whelan, D T Producer: 19970102 In: European journal of human genetics : EJHG vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency.. [electronic resource] by Nowaczyk, M J Huggins, M J Tomkins, D J Rossi, E Ramsay, J A Woulfe, J Scherer, S W Belloni, E Producer: 20000928 In: Clinical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Canadian multicenter randomized clinical trial of chorion villus sampling and amniocentesis. List of all cytogenetic abnormalities detected. [electronic resource] by Tomkins, D J Vekemans, M J Teshima, I E Cox, D M Dallaire, L Gagne, R Kalousek, D K Lin, J C Markovic, V D Ray, M Producer: 19921014 In: Prenatal diagnosis vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT). [electronic resource] by Winsor, E J Tomkins, D J Kalousek, D Farrell, S Wyatt, P Fan, Y S Carter, R Wang, H Dallaire, L Eydoux, P Welch, J P Dawson, A Lin, J C Singer, J Johnson, J Wilson, R D Producer: 19990819 In: Prenatal diagnosis vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia. [electronic resource] by Chen, M Tomkins, D J Auerbach, W McKerlie, C Youssoufian, H Liu, L Gan, O Carreau, M Auerbach, A Groves, T Guidos, C J Freedman, M H Cross, J Percy, D H Dick, J E Joyner, A L Buchwald, M Producer: 19960703 In: Nature genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)