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Results: 5

Authors: PRAMSTALLER PP KLEIN C CASTELLAN C BREAKEFIELD XO OZELIUS LJ
Citation: Pp. Pramstaller et al., CLINICAL AND GENETIC-CHARACTERIZATION OF A FAMILY FROM SOUTH TYROL (NORTHERN ITALY) WITH AN UNUSUAL PRESENTATION OF DYSTONIA, Neurology, 50(4), 1998, pp. 2027-2027

Authors: MERIENNE K JACQUOT S TRIVIER E PANNETIER S ROSSI A SCOTT C SCHINZEL A CASTELLAN C KRESS W HANAUER A
Citation: K. Merienne et al., RAPID IMMUNOBLOT AND KINASE ASSAY TESTS FOR A SYNDROMAL FORM OF X-LINKED MENTAL-RETARDATION - COFFIN-LOWRY-SYNDROME, Journal of Medical Genetics, 35(11), 1998, pp. 890-894

Authors: KOTZOT D BUNDSCHERER G BERNASCONI F BRECEVIC L LURIE IW BASARAN S BACCICCHETTI C HOLLER A CASTELLAN C BRAUNQUENTIN C PFEIFFER RA SCHINZEL A
Citation: D. Kotzot et al., ISOCHROMOSOME 18P RESULTS FROM MATERNAL MEIOSIS-II NONDISJUNCTION, European journal of human genetics, 4(3), 1996, pp. 168-174

Authors: LURIE IW ILYINA HG GUREVICH DB RUMYANTSEVA NV NAUMCHIK IV CASTELLAN C HOELLER A SCHINZEL A
Citation: Iw. Lurie et al., TRISOMY 2P - ANALYSIS OF UNUSUAL PHENOTYPIC FINDINGS, American journal of medical genetics, 55(2), 1995, pp. 229-236

Authors: RADETTI G CASTELLAN C TATO L PLATTER K GENTILI L ADAMI S
Citation: G. Radetti et al., BONE-MINERAL DENSITY IN CHILDREN AND ADOLESCENT FEMALES TREATED WITH HIGH-DOSES OF L-THYROXINE, Hormone research, 39(3-4), 1993, pp. 127-131
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