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J A Hurst

Showing results (21-30 of 44) with videos related to

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The Medical Journal of Australia|June 11, 1977
Urinary tract infections in childhood: the place of the nitrite testI J Skelton, M M Hogan, B Stokes, et al.
Developmental Medicine and Child Neurology|April 1, 1990
An extended family with a dominantly inherited speech disorderJ A Hurst, M Baraitser, E Auger, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|May 25, 2005
UV-vis spectroscopic study of Co(II)/Co(III) oxidation in poly[M-protoporphyrins] films and their interaction with axial ligandsV Campo Dall' Orto, R Carballo, J A Hurst, et al.
American Journal of Ophthalmology|June 1, 1995
Duane's retraction syndrome associated with chromosome 4q27-31 segment deletionC K Chew, P Foster, J A Hurst, et al.
Clinical Genetics|April 29, 1998
ACTH receptor mutation in a girl with familial glucocorticoid deficiencyA M Slavotinek, J A Hurst, D Dunger, et al.
Journal of Medical Genetics|January 1, 1990
De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomaliesI K Temple, J A Hurst, S Hing, et al.
American Journal of Medical Genetics|February 24, 2001
Renal-hepatic-pancreatic dysplasia: a broad entityS M White, J A Hurst, H Hamoda, et al.
Journal of Medical Genetics|August 6, 2000
Two further cases of Sener syndrome: frontonasal dysplasia and dilated Virchow-Robin spacesS A Lynch, K Hall, S Precious, et al.
American Journal of Medical Genetics|September 11, 1995
Geleophysic dysplasia: a report of three affected boys--prenatal ultrasound does not detect recurrenceE M Rosser, A R Wilkinson, J A Hurst, et al.
Clinical Dysmorphology|October 1, 1995
Transverse limb deficiency, facial clefting and hypoxic renal damage: an association with treatment of maternal hypertension?J A Hurst, R S Houlston, A Roberts, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
The Medical Journal of Australia|June 11, 1977
Urinary tract infections in childhood: the place of the nitrite testI J Skelton, M M Hogan, B Stokes, et al.
Developmental Medicine and Child Neurology|April 1, 1990
An extended family with a dominantly inherited speech disorderJ A Hurst, M Baraitser, E Auger, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|May 25, 2005
UV-vis spectroscopic study of Co(II)/Co(III) oxidation in poly[M-protoporphyrins] films and their interaction with axial ligandsV Campo Dall' Orto, R Carballo, J A Hurst, et al.
American Journal of Ophthalmology|June 1, 1995
Duane's retraction syndrome associated with chromosome 4q27-31 segment deletionC K Chew, P Foster, J A Hurst, et al.
Clinical Genetics|April 29, 1998
ACTH receptor mutation in a girl with familial glucocorticoid deficiencyA M Slavotinek, J A Hurst, D Dunger, et al.
Journal of Medical Genetics|January 1, 1990
De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomaliesI K Temple, J A Hurst, S Hing, et al.
American Journal of Medical Genetics|February 24, 2001
Renal-hepatic-pancreatic dysplasia: a broad entityS M White, J A Hurst, H Hamoda, et al.
Journal of Medical Genetics|August 6, 2000
Two further cases of Sener syndrome: frontonasal dysplasia and dilated Virchow-Robin spacesS A Lynch, K Hall, S Precious, et al.
American Journal of Medical Genetics|September 11, 1995
Geleophysic dysplasia: a report of three affected boys--prenatal ultrasound does not detect recurrenceE M Rosser, A R Wilkinson, J A Hurst, et al.
Clinical Dysmorphology|October 1, 1995
Transverse limb deficiency, facial clefting and hypoxic renal damage: an association with treatment of maternal hypertension?J A Hurst, R S Houlston, A Roberts, et al.
Pageof 5