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S Gaillez

Showing results (1-10 of 5) with videos related to

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Revue Medicale De Liege|July 30, 2013
[Are we genetically predisposed to addictions?]E Castermans, S Gaillez, V Bours
Revue Medicale De Liege|May 13, 2011
[X-linked hydrocephaly. A case report in fetal medicine]K Syrios, K Delbecoue, S Gaillez, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13A Uwineza, G Pierquin, S Gaillez, et al.
Revue Medicale De Liege|October 6, 2006
[Prader-Willi syndrome: specific management by a multidisciplinary team]C Salmon, S Gaillez, C Pieltain, et al.
Clinical Genetics|April 2, 2015
Diagnostic pitfall in antenatal manifestations of CPT II deficiencyF Boemer, M Deberg, R Schoos, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Revue Medicale De Liege|July 30, 2013
[Are we genetically predisposed to addictions?]E Castermans, S Gaillez, V Bours
Revue Medicale De Liege|May 13, 2011
[X-linked hydrocephaly. A case report in fetal medicine]K Syrios, K Delbecoue, S Gaillez, et al.
Genetic Counseling (Geneva, Switzerland)|September 17, 2013
Clinical, cytogenetic and molecular characterization of two cases of mosaic ring chromosome 13A Uwineza, G Pierquin, S Gaillez, et al.
Revue Medicale De Liege|October 6, 2006
[Prader-Willi syndrome: specific management by a multidisciplinary team]C Salmon, S Gaillez, C Pieltain, et al.
Clinical Genetics|April 2, 2015
Diagnostic pitfall in antenatal manifestations of CPT II deficiencyF Boemer, M Deberg, R Schoos, et al.
Pageof 1