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Isil Halac

Showing results (1-10 of 7) with videos related to

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Pediatric Annals|April 2, 2004
Coordinating care for children with Turner syndromeIsil Halac, Donald Zimmerman
Pediatric Annals|April 2, 2004
Evaluating short stature in childrenIsil Halac, Donald Zimmerman
Endocrinology and Metabolism Clinics of North America|August 9, 2005
Thyroid nodules and cancers in childrenIsil Halac, Donald Zimmerman
Pediatric Annals|April 2, 2004
Managing growth hormone treatment in pediatric patientsIsil Halac, Donald Zimmerman
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 28, 2005
Endocrine manifestations of craniopharyngiomaIsil Halac, Donald Zimmerman
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 26, 2006
Central and gonadal hypogonadism in X-linked lissencephalyIsil Halac, Reema Habiby, John Curran, et al.
Human Molecular Genetics|January 11, 2007
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factorAsif Ali, Paul T Christie, Irina V Grigorieva, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Pediatric Annals|April 2, 2004
Coordinating care for children with Turner syndromeIsil Halac, Donald Zimmerman
Pediatric Annals|April 2, 2004
Evaluating short stature in childrenIsil Halac, Donald Zimmerman
Endocrinology and Metabolism Clinics of North America|August 9, 2005
Thyroid nodules and cancers in childrenIsil Halac, Donald Zimmerman
Pediatric Annals|April 2, 2004
Managing growth hormone treatment in pediatric patientsIsil Halac, Donald Zimmerman
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 28, 2005
Endocrine manifestations of craniopharyngiomaIsil Halac, Donald Zimmerman
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 26, 2006
Central and gonadal hypogonadism in X-linked lissencephalyIsil Halac, Reema Habiby, John Curran, et al.
Human Molecular Genetics|January 11, 2007
Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcription factorAsif Ali, Paul T Christie, Irina V Grigorieva, et al.
Pageof 1