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Showing results (61-70 of 82) with videos related to

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Journal of Endocrinological Investigation|January 28, 2014
Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literatureM Agopiantz, P Corbonnois, A Sorlin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 1, 1994
[Final height in Turner syndrome treated with growth hormone]P Rocchiccioli, J Battin, A M Bertrand, et al.
Molecular Genetics and Metabolism Reports|October 21, 2016
30 months follow-up of an early enzyme replacement therapy in a severe Morquio A patient: About one caseJ Do Cao, A Wiedemann, T Quinaux, et al.
Bone Marrow Transplantation|November 18, 2008
Height growth during adolescence and final height after haematopoietic SCT for childhood acute leukaemia: the impact of a conditioning regimen with BU or TBIF Bernard, P Bordigoni, M-C Simeoni, et al.
Clinical Genetics|July 4, 2006
Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndromeC Badens, C Lacoste, N Philip, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Confirmation of TFAP2A gene involvement in branchio-oculo-facial syndrome (BOFS) and report of temporal bone anomaliesC Stoetzel, S Riehm, V Bennouna Greene, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
Three-year data from a comparative study with recombinant human growth hormone in the treatment of short stature in young children with intrauterine growth retardationA Fjellestad-Paulsen, P Czernichow, R Brauner, et al.
Journal of Medical Genetics|February 24, 2001
The mutation spectrum in Holt-Oram syndromeS J Cross, Y H Ching, Q Y Li, et al.
Journal of Medical Genetics|November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experienceB Keren, A Hadchouel, S Saba, et al.
Molecular Syndromology|October 30, 2013
Array-CGH Analysis Suggests Genetic Heterogeneity in RhombencephalosynapsisF Démurger, L Pasquier, C Dubourg, et al.
Pageof 9

Showing results (61-70 of 82) with videos related to

Sort By:
Pageof 9
Journal of Endocrinological Investigation|January 28, 2014
Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literatureM Agopiantz, P Corbonnois, A Sorlin, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 1, 1994
[Final height in Turner syndrome treated with growth hormone]P Rocchiccioli, J Battin, A M Bertrand, et al.
Molecular Genetics and Metabolism Reports|October 21, 2016
30 months follow-up of an early enzyme replacement therapy in a severe Morquio A patient: About one caseJ Do Cao, A Wiedemann, T Quinaux, et al.
Bone Marrow Transplantation|November 18, 2008
Height growth during adolescence and final height after haematopoietic SCT for childhood acute leukaemia: the impact of a conditioning regimen with BU or TBIF Bernard, P Bordigoni, M-C Simeoni, et al.
Clinical Genetics|July 4, 2006
Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndromeC Badens, C Lacoste, N Philip, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Confirmation of TFAP2A gene involvement in branchio-oculo-facial syndrome (BOFS) and report of temporal bone anomaliesC Stoetzel, S Riehm, V Bennouna Greene, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
Three-year data from a comparative study with recombinant human growth hormone in the treatment of short stature in young children with intrauterine growth retardationA Fjellestad-Paulsen, P Czernichow, R Brauner, et al.
Journal of Medical Genetics|February 24, 2001
The mutation spectrum in Holt-Oram syndromeS J Cross, Y H Ching, Q Y Li, et al.
Journal of Medical Genetics|November 3, 2004
PTPN11 mutations in patients with LEOPARD syndrome: a French multicentric experienceB Keren, A Hadchouel, S Saba, et al.
Molecular Syndromology|October 30, 2013
Array-CGH Analysis Suggests Genetic Heterogeneity in RhombencephalosynapsisF Démurger, L Pasquier, C Dubourg, et al.
Pageof 9