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Results: 1-25 | 26-33 |
Results: 26-33/33
Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin
Authors: van der Loop, FTL Monnens, LAH Schroder, CH Lemmink, HH Breuning, MH Timmer, EDJ Smeets, HJM
Citation: Ftl. Van Der Loop et al., Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin, KIDNEY INT, 55(4), 1999, pp. 1217-1224
Diagnostic Notch3 sequence analysis in CADASIL: Three new mutations in Dutch patients
Authors: Oberstein, SAJL Ferrari, MD Bakker, E van Gestel, J Kneppers, ALJ Frants, RR Breuning, MH Haan, J
Citation: Sajl. Oberstein et al., Diagnostic Notch3 sequence analysis in CADASIL: Three new mutations in Dutch patients, NEUROLOGY, 52(9), 1999, pp. 1913-1915
Cellular localization and tissue distribution of polycystin-1
Authors: Peters, DJM Van de Wal, A Spruit, L Saris, JJ Breuning, MH Bruijn, JA De Heer, E
Citation: Djm. Peters et al., Cellular localization and tissue distribution of polycystin-1, J PATHOLOGY, 188(4), 1999, pp. 439-446
A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome)
Authors: Brooks, AS Breuning, MH Osinga, J Van der Smagt, JJ Catsman, CE Buys, CHCM Meijers, C Hofstra, RMW
Citation: As. Brooks et al., A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome), J MED GENET, 36(6), 1999, pp. 485-489
Two-colour FISH detection of the inv(16) in interphase nuclei of patients with acute myeloid leukaemia
Authors: Dauwerse, HG Smit, EME Giles, RH Slater, R Breuning, MH Hagemijer, A van der Reijden, BA
Citation: Hg. Dauwerse et al., Two-colour FISH detection of the inv(16) in interphase nuclei of patients with acute myeloid leukaemia, BR J HAEM, 106(1), 1999, pp. 111-114
The 782C -> T (T254M) XHIM mutation: Lack of a tight phenotype-genotype relationship
Authors: de Vries, E Noordzij, JG Davies, EG Hartwig, N Breuning, MH van Dongen, JJM van Tol, MJD
Citation: E. De Vries et al., The 782C -> T (T254M) XHIM mutation: Lack of a tight phenotype-genotype relationship, BLOOD, 94(4), 1999, pp. 1488-1489
Molecular analysis of SALL1 mutations in Townes-Brocks syndrome
Authors: Kohlhase, J Taschner, PEM Burfeind, P Pasche, B Newman, B Blanck, C Breuning, MH ten Kate, LP Maaswinkel-Mooy, P Mitulla, B Seidel, J Kirkpatrick, SJ Pauli, RM Wargowski, DS Devriendt, K Proesmans, W Gabrielli, O Coppa, GV Wesby-van Swaay, E Trembath, RC Schinzel, AA Reardon, W Seemanova, E Engel, W
Citation: J. Kohlhase et al., Molecular analysis of SALL1 mutations in Townes-Brocks syndrome, AM J HU GEN, 64(2), 1999, pp. 435-445
Physical mapping of the short arm of human chromosome 16
Authors: Mole, SE Breuning, MH Ceccherini, I Harris, PC Lushnikova, T
Citation: Se. Mole et al., Physical mapping of the short arm of human chromosome 16, BIOM HLTH R, 23, 1998, pp. 129-149
Risultati: 1-25 | 26-33 |