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SYMPTOMATOLOGIE DER AKUTEN AORTENDISSEKTION. BEOBACHTUNGEN AN SECHS FAELLEN = SYMPTOMATOLOGIE DE LA DISSECTION AORTIQUE AIGUE. OBSERVATION DE 6 CASKRESBACH E; THURNHER H; SCHUMACHER V et al.1972; MED. KLIN.; DTSCH.; DA. 1972; VOL. 67; NO 47; PP. 1554-1558; ABS. ANGL.; BIBL. 27 REF.Serial Issue

Früher neonataler Tod bei Drash-Syndrom = Early neonatal death in Drash syndromeGUSCHMANN, M; VOGEL, M; SCHUMACHER, V et al.Monatsschrift für Kinderheilkunde. 1998, Vol 146, Num 7, pp 683-686, issn 0026-9298Article

Chromosome painting in highly irradiated Chernobyl victims : a follow-up study to evaluate the stability of symmetrical translocations and the influence of clonal aberrations for retrospective dose estimationSALASSIDIS, K; GEORGIADOU-SCHUMACHER, V; BRASELMANN, H et al.International journal of radiation biology (Print). 1995, Vol 68, Num 3, pp 257-262, issn 0955-3002Conference Paper

Quantification of FISH-painted chromosome aberrations after domestic radon exposureBAUCHINGER, M; BRASELMANN, H; KULKA, U et al.International journal of radiation biology (Print). 1996, Vol 70, Num 6, pp 657-663, issn 0955-3002Article

Transfusions foetales intra-utérines = In utero transfusionsSCHUMACHER, V; VIAL, Y; TISSOT, J. D et al.Médecine et hygiène. 1997, Vol 55, Num 2162, pp 938-944, issn 0025-6749, 4 p.Article

Identification of Lipoprotein Ms1A as a Neoteric Virulence Factor of Mycoplasma gallisepticumSZCZEPANEK, S. M; FRASCA, S; SCHUMACHER, V. L et al.Infection and immunity. 2010, Vol 78, Num 8, pp 3475-3483, issn 0019-9567, 9 p.Article

STK11 genotyping and cancer risk in Peutz-Jeghers syndromeSCHUMACHER, V; VOGEL, T; LEUBE, B et al.Journal of medical genetics. 2005, Vol 42, Num 5, pp 428-435, issn 0022-2593, 8 p.Article

Genomic structure, alternative transcripts and chromosome location of the human LIM domain binding protein 1 gene LDB1DRECHSLER, M; SCHUMACHER, V; FRIEDRICH, S et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 1-2, pp 119-124, issn 0301-0171Article

A high proportion of mutations in the BRCA1 gene in German breast/ovarian cancer families with clustering of mutations in the 3'third of the geneJUAN DONG; CHANG-CLAUDE, J; YIXIN WU et al.Human genetics. 1998, Vol 103, Num 2, pp 154-161, issn 0340-6717Article

Analysis of the combustion process of a spark ignition engine with a variable compression ratioADAMS, W. H; HINRICHS, H. G; PISCHINGER, F. F et al.SAE transactions. 1987, Vol 96, Num 4, pp 749-757, issn 0096-736XArticle

Bilateral Wilms tumor in a boy with severe hypospadias and cryptorchidism due to a heterozygous mutation in the WT1 geneKÖHLER, B; SCHUMACHER, V; SCHULTE-OVERBERG, U et al.Pediatric research. 1999, Vol 45, Num 2, pp 187-190, issn 0031-3998Article

Chromosome translocations in thyroid tissues from Belarussian children exposed to radioiodine from the Chernobyl accident, measured by FISH-paintingLEHMANN, L; ZITZELSBERGER, H; BAUCHINGER, M et al.International journal of radiation biology (Print). 1996, Vol 70, Num 5, pp 513-516, issn 0955-3002Article

Toxicity of Santander Bay sediments to the euryhaline freshwater oligochaete Limnodrilus hoffmeisteriRODRIGUEZ, P; ARRATE, J; MARTINEZ-MADRID, M et al.Hydrobiologia (The Hague). 2006, Vol 564, pp 157-169, issn 0018-8158, 13 p.Conference Paper

Spectrum of early onset nephrotic syndrome associated with WT1 missense mutationsSCHUMACHER, V; SCHÄRER, K; TONDERA, A.-M et al.Kidney international. 1998, Vol 53, Num 6, pp 1594-1600, issn 0085-2538Conference Paper

Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2RAPLEY, E. A; BARFOOT, R; SKEEN, J et al.British journal of cancer. 2000, Vol 83, Num 2, pp 177-183, issn 0007-0920Article

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders. CommentaryDANDAPANI, S. V; POLLAK, M. R; BECKER, C et al.Kidney international. 2006, Vol 70, Num 6, issn 0085-2538, 980-982,1008-1012 [8 p.]Article