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G Pierquin

Showing results (1-10 of 17) with videos related to

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Journal De Genetique Humaine|September 1, 1985
[Fetal or neonatal autopsy and genetic counseling. Experience of the Human Genetic Service of Liège]G Pierquin, P Dodinval
Journal De Genetique Humaine|December 1, 1988
[Supravalvular aortic stenosis. Autosomal dominant form of congenital cardiopathy]G Pierquin, A Vliers, P Dodinval
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Familial occurrence of Summitt syndrome or a variant example of Carpenter syndrome?G Pierquin, R Seligmann, N Van Regemorter
Ophthalmic Paediatrics and Genetics|December 1, 1991
A new case of acro-renal-ocular (radio-renal-ocular) syndrome with cleft palate and costo-vertebral defects? A brief clinical reportG Pierquin, M Hall, C Vanhelleputte, et al.
Revue Medicale De Liege|May 22, 2007
[Hutchinson-Gilford progeria syndrome: clinical and molecular analysis in an African patient]L Mutesa, G Pierquin, N Cwiny-Ay, et al.
Prenatal Diagnosis|May 1, 1989
Mosaicism of 46,XX/47,XX,+9/47,XX,+?mar in the same amniotic fluid with apparent loss of one cell line after deliveryC Herens, G Pierquin, A Verloes, et al.
Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Need for search for cryptic translocation in parents with several children affected with MCA: report of a cryptic translocation (10;14) detected by FISHD Delneste, E Vamos, G Pierquin, et al.
Genetic Counseling (Geneva, Switzerland)|August 23, 2007
Precocious puberty associated with partial trisomy 18q and monosomy 11qL Mutesa, A C Hellin, M Jamar, et al.
American Journal of Medical Genetics|August 1, 1989
Dandy-Walker malformation with postaxial polydactyly: a new syndrome?G Pierquin, J Deroover, S Levi, et al.
Clinical Genetics|May 1, 1988
Partial trisomy 20q due to paternal t(8;20) translocation. Case report and review of the literatureG Pierquin, C Herens, P Dodinval, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Journal De Genetique Humaine|September 1, 1985
[Fetal or neonatal autopsy and genetic counseling. Experience of the Human Genetic Service of Liège]G Pierquin, P Dodinval
Journal De Genetique Humaine|December 1, 1988
[Supravalvular aortic stenosis. Autosomal dominant form of congenital cardiopathy]G Pierquin, A Vliers, P Dodinval
Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Familial occurrence of Summitt syndrome or a variant example of Carpenter syndrome?G Pierquin, R Seligmann, N Van Regemorter
Ophthalmic Paediatrics and Genetics|December 1, 1991
A new case of acro-renal-ocular (radio-renal-ocular) syndrome with cleft palate and costo-vertebral defects? A brief clinical reportG Pierquin, M Hall, C Vanhelleputte, et al.
Revue Medicale De Liege|May 22, 2007
[Hutchinson-Gilford progeria syndrome: clinical and molecular analysis in an African patient]L Mutesa, G Pierquin, N Cwiny-Ay, et al.
Prenatal Diagnosis|May 1, 1989
Mosaicism of 46,XX/47,XX,+9/47,XX,+?mar in the same amniotic fluid with apparent loss of one cell line after deliveryC Herens, G Pierquin, A Verloes, et al.
Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Need for search for cryptic translocation in parents with several children affected with MCA: report of a cryptic translocation (10;14) detected by FISHD Delneste, E Vamos, G Pierquin, et al.
Genetic Counseling (Geneva, Switzerland)|August 23, 2007
Precocious puberty associated with partial trisomy 18q and monosomy 11qL Mutesa, A C Hellin, M Jamar, et al.
American Journal of Medical Genetics|August 1, 1989
Dandy-Walker malformation with postaxial polydactyly: a new syndrome?G Pierquin, J Deroover, S Levi, et al.
Clinical Genetics|May 1, 1988
Partial trisomy 20q due to paternal t(8;20) translocation. Case report and review of the literatureG Pierquin, C Herens, P Dodinval, et al.
Pageof 2