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P Soothill

Showing results (31-40 of 37) with videos related to

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Pediatric Research|May 1, 1996
First trimester prenatal diagnosis of Smith-Lemli-Opitz syndrome (7-dehydrocholesterol reductase deficiency)K Mills, H Mandel, R Montemagno, et al.
Lancet (London, England)|February 4, 1995
Prenatal detection of fetal RhD DNA sequences in transcervical samplesM Adinolfi, J Sherlock, T Kemp, et al.
Journal of Anatomy|April 1, 1996
Matrix metalloproteinases in the formation of human synovial joint cavitiesJ C Edwards, L S Wilkinson, P Soothill, et al.
Molecular and Cellular Endocrinology|April 28, 1995
KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human developmentV M Duke, P J Winyard, P Thorogood, et al.
Journal of Anatomy|October 1, 1994
The formation of human synovial joint cavities: a possible role for hyaluronan and CD44 in altered interzone cohesionJ C Edwards, L S Wilkinson, H M Jones, et al.
Placenta|December 28, 2010
Pregenesys pre-eclampsia markers consensus meeting: What do we require from markers, risk assessment and model systems to tailor preventive strategies?I Cetin, B Huppertz, G Burton, et al.
Community Genetics|July 11, 2002
Counselling following the Prenatal Diagnosis of Klinefelter Syndrome: Comparisons between Geneticists and Obstetricians in Five European CountriesS. Hall, T.M. Marteau, C. Limbert, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Pediatric Research|May 1, 1996
First trimester prenatal diagnosis of Smith-Lemli-Opitz syndrome (7-dehydrocholesterol reductase deficiency)K Mills, H Mandel, R Montemagno, et al.
Lancet (London, England)|February 4, 1995
Prenatal detection of fetal RhD DNA sequences in transcervical samplesM Adinolfi, J Sherlock, T Kemp, et al.
Journal of Anatomy|April 1, 1996
Matrix metalloproteinases in the formation of human synovial joint cavitiesJ C Edwards, L S Wilkinson, P Soothill, et al.
Molecular and Cellular Endocrinology|April 28, 1995
KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human developmentV M Duke, P J Winyard, P Thorogood, et al.
Journal of Anatomy|October 1, 1994
The formation of human synovial joint cavities: a possible role for hyaluronan and CD44 in altered interzone cohesionJ C Edwards, L S Wilkinson, H M Jones, et al.
Placenta|December 28, 2010
Pregenesys pre-eclampsia markers consensus meeting: What do we require from markers, risk assessment and model systems to tailor preventive strategies?I Cetin, B Huppertz, G Burton, et al.
Community Genetics|July 11, 2002
Counselling following the Prenatal Diagnosis of Klinefelter Syndrome: Comparisons between Geneticists and Obstetricians in Five European CountriesS. Hall, T.M. Marteau, C. Limbert, et al.
Pageof 4