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Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|October 26, 2010
The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal ageA Hagen, M Entezami, A Gasiorek-Wiens, et al.
Cancer|March 1, 1994
Low-grade non-Hodgkin's lymphoma after high-grade non-Hodgkin's lymphoma in a child with ataxia telangiectasiaU Overberg-Schmidt, R D Wegner, E Baumgarten, et al.
Clinical Genetics|January 1, 1988
A new chromosomal instability disorder confirmed by complementation studiesR D Wegner, M Metzger, F Hanefeld, et al.
Acta Haematologica|January 1, 1989
Calla-positive acute leukaemia with t(5q;14q) translocation and hypereosinophilia--a unique entity?E Baumgarten, R D Wegner, R Fengler, et al.
Reproduction in Domestic Animals = Zuchthygiene|April 24, 2010
Dystocia and fetotomy associated with cerebral aplasia in a greater one-horned rhinoceros (Rhinoceros unicornis)W Schaftenaar, T Fernandes, G Fritsch, et al.
Clinical Genetics|May 1, 1997
Linkage studies exclude the AT-V gene(s) from the translocation breakpoints in an AT-V patientK Chrzanowska, M Stumm, M Bialecka, et al.
Prenatal Diagnosis|October 7, 2010
A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator datasetA Gasiorek-Wiens, S Kotsis, I Staboulidou, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Localisation of a Fanconi anaemia gene to chromosome 9pK Saar, D Schindler, R D Wegner, et al.
Clinical Genetics|July 1, 1986
Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative studyA Rodewald, U Froster-Iskenius, E Käb, et al.
Human Genetics|November 1, 1995
DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factorS Schuffenhauer, O Bartsch, M Stumm, et al.
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