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Results: 4

Authors: VANBOKHOVEN H KISSING J SCHEPENS M VANBEERSUM S SIMONS A RIEGMAN P MCMAHON JA MCMAHON AP BRUNNER HG
Citation: H. Vanbokhoven et al., ASSIGNMENT OF WNT7B TO HUMAN-CHROMOSOME BAND 22Q13 BY IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 77(3-4), 1997, pp. 288-289

Authors: GABREELSFESTEN AAWM HOOGENDIJK JE MEIJERINK PHS GABREELS FJM BOLHUIS PA VANBEERSUM S KULKENS T NELIS E JENNEKENS FGI DEVISSER M VANENGELEN BGM VANBROECKHOVEN C MARIMAN ECM
Citation: Aawm. Gabreelsfesten et al., 2 DIVERGENT TYPES OF NERVE PATHOLOGY IN PATIENTS WITH DIFFERENT P-0 MUTATIONS IN CHARCOT-MARIE-TOOTH DISEASE, Neurology, 47(3), 1996, pp. 761-765

Authors: VANDERBURGT I BERENDS E LOMMEN E VANBEERSUM S HAMEL B MARIMAN E
Citation: I. Vanderburgt et al., CLINICAL AND MOLECULAR STUDIES IN A LARGE DUTCH FAMILY WITH NOONAN SYNDROME, American journal of medical genetics, 53(2), 1994, pp. 187-191

Authors: MARIMAN E GABREELSFESTEN A VANBEERSUM S JONGEN P GABREELS F ROPERS HH
Citation: E. Mariman et al., GENETIC AND MOLECULAR ANALYSIS OF FAMILIES WITH HEREDITARY NEUROPATHYWITH LIABILITY TO PRESSURE PALSIES, American journal of human genetics, 53(3), 1993, pp. 1041-1041
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