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Acta Universitatis Carolinae. Medica|January 1, 1990
Cystic fibrosis marker testing in Bohemia with polymerase chain reactionM Macek, I Böhm, L Arnold, et al.
Casopis Lekaru Ceskych|May 11, 1990
[Experience with rapid molecular genetic diagnosis using the polymerase chain reaction]M Macek, I Böhm, L Arnold, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|March 24, 1998
A murine TSPYT Vogel, H Boettger-Tong, I Nanda, et al.
British Journal of Haematology|March 22, 2001
Familial thrombocytosis as a recessive, possibly X-linked trait in an Arab familyM Stuhrmann, L Bashawri, M A Ahmed, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|October 14, 2011
pH-dependent spectral properties of para-aminobenzoic acid and its derivativesMitchell P Thayer, Colin McGuire, Elana M S Stennett, et al.
Neurology|February 1, 1995
The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigreesP G Barth, G Blennow, H G Lenard, et al.
European Journal of Pediatrics|October 1, 1992
Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromesH Seyschab, D Schindler, R Friedl, et al.
International Journal of Oral and Maxillofacial Surgery|May 6, 2003
Search for deletion 22q11.2 in interphase nuclei of buccal mucosa of patients ascertained by isolated cleft palate: a new diagnostic approachN Shouman, B Pabst, M Arslan-Kirchner, et al.
Familial Cancer|March 15, 2011
Familial breast cancer: is it time to move from a reactive to a proactive role?H Harris, I Nippert, C Julian-Reynier, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric acidaemia: clinical and biochemical findings in 12 patients and preliminary report on L-2-hydroxyacid dehydrogenaseP G Barth, G F Hoffmann, J Jaeken, et al.
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