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J C Dean

Showing results (61-70 of 111) with videos related to

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Journal of Medical Genetics|June 1, 1992
Cardiofaciocutaneous syndrome with new ectodermal manifestationsP D Turnpenny, J C Dean, I A Auchterlonie, et al.
Clinical Radiology|March 2, 1999
Protrusio acetabuli in Marfan's syndromeS R Yule, E E Hobson, J C Dean, et al.
Journal of Medical Genetics|August 1, 1991
Facial dysmorphism: a marker of autosomal dominant cranial diabetes insipidusR B Laing, J C Dean, D W Pearson, et al.
Lancet (London, England)|April 6, 1996
Cystic fibrosis screening policiesM H Hall, Z H Miedzybrodzka, N E Haites, et al.
The British Journal of Ophthalmology|February 1, 1993
The Farnsworth-Munsell 100 hue test in the first episode of demyelinating optic neuritisM J Ménage, D Papakostopoulos, J C Dean Hart, et al.
Muscle & Nerve|October 31, 2000
Measurement of central activation failure of the quadriceps femoris in healthy adultsS K Stackhouse, J C Dean, S C Lee, et al.
Journal of Medical Genetics|September 19, 2000
Genetic registers in clinical practice: a survey of UK clinical geneticsJ C Dean, D R Fitzpatrick, P A Farndon, et al.
Clinical Genetics|November 24, 1999
Fetal anticonvulsant syndrome and mutation in the maternal MTHFR geneJ C Dean, S J Moore, A Osborne, et al.
Journal of Medical Genetics|September 1, 1992
Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defectsP D Turnpenny, J C Dean, P Duffty, et al.
Thorax|June 13, 1998
Withdrawn: Opitz oculo-genito-laryngeal syndrome: a rare cause of recurrent aspiration pneumonia in an adultD de Silva, A Osborne, S A Simpson, et al.
Pageof 12

Showing results (61-70 of 111) with videos related to

Sort By:
Pageof 12
Journal of Medical Genetics|June 1, 1992
Cardiofaciocutaneous syndrome with new ectodermal manifestationsP D Turnpenny, J C Dean, I A Auchterlonie, et al.
Clinical Radiology|March 2, 1999
Protrusio acetabuli in Marfan's syndromeS R Yule, E E Hobson, J C Dean, et al.
Journal of Medical Genetics|August 1, 1991
Facial dysmorphism: a marker of autosomal dominant cranial diabetes insipidusR B Laing, J C Dean, D W Pearson, et al.
Lancet (London, England)|April 6, 1996
Cystic fibrosis screening policiesM H Hall, Z H Miedzybrodzka, N E Haites, et al.
The British Journal of Ophthalmology|February 1, 1993
The Farnsworth-Munsell 100 hue test in the first episode of demyelinating optic neuritisM J Ménage, D Papakostopoulos, J C Dean Hart, et al.
Muscle & Nerve|October 31, 2000
Measurement of central activation failure of the quadriceps femoris in healthy adultsS K Stackhouse, J C Dean, S C Lee, et al.
Journal of Medical Genetics|September 19, 2000
Genetic registers in clinical practice: a survey of UK clinical geneticsJ C Dean, D R Fitzpatrick, P A Farndon, et al.
Clinical Genetics|November 24, 1999
Fetal anticonvulsant syndrome and mutation in the maternal MTHFR geneJ C Dean, S J Moore, A Osborne, et al.
Journal of Medical Genetics|September 1, 1992
Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defectsP D Turnpenny, J C Dean, P Duffty, et al.
Thorax|June 13, 1998
Withdrawn: Opitz oculo-genito-laryngeal syndrome: a rare cause of recurrent aspiration pneumonia in an adultD de Silva, A Osborne, S A Simpson, et al.
Pageof 12