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T Homfray

Showing results (11-20 of 30) with videos related to

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Prenatal Diagnosis|March 24, 2007
Outcome of prenatally diagnosed agenesis of the corpus callosumN Fratelli, A T Papageorghiou, F Prefumo, et al.
Journal of Medical Genetics|January 11, 2000
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)W Wuyts, E Cleiren, T Homfray, et al.
Journal of Medical Genetics|January 1, 1997
Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancerI P Tomlinson, N E Beck, T Homfray, et al.
The British Journal of Surgery|February 1, 1997
Genetic testing is important in families with a history suggestive of hereditary non-polyposis colorectal cancer even if the Amsterdam criteria are not fulfilledN E Beck, I P Tomlinson, T Homfray, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 2, 2012
Counseling in fetal medicine: agenesis of the corpus callosumS Santo, F D'Antonio, T Homfray, et al.
Human Genetics|February 1, 1997
Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteriaN E Beck, I P Tomlinson, T Homfray, et al.
Human Molecular Genetics|April 18, 2000
Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagnaW Wuyts, W Reardon, S Preis, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 21, 2020
Non-immune fetal hydrops: etiology and outcome according to gestational age at diagnosisF G Sileo, A Kulkarni, I Branescu, et al.
Lancet (London, England)|November 24, 1999
Subtle chromosomal rearrangements in children with unexplained mental retardationS J Knight, R Regan, A Nicod, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|September 27, 2020
A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective reviewE Dempsey, A Haworth, L Ive, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Prenatal Diagnosis|March 24, 2007
Outcome of prenatally diagnosed agenesis of the corpus callosumN Fratelli, A T Papageorghiou, F Prefumo, et al.
Journal of Medical Genetics|January 11, 2000
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)W Wuyts, E Cleiren, T Homfray, et al.
Journal of Medical Genetics|January 1, 1997
Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancerI P Tomlinson, N E Beck, T Homfray, et al.
The British Journal of Surgery|February 1, 1997
Genetic testing is important in families with a history suggestive of hereditary non-polyposis colorectal cancer even if the Amsterdam criteria are not fulfilledN E Beck, I P Tomlinson, T Homfray, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 2, 2012
Counseling in fetal medicine: agenesis of the corpus callosumS Santo, F D'Antonio, T Homfray, et al.
Human Genetics|February 1, 1997
Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteriaN E Beck, I P Tomlinson, T Homfray, et al.
Human Molecular Genetics|April 18, 2000
Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagnaW Wuyts, W Reardon, S Preis, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|March 21, 2020
Non-immune fetal hydrops: etiology and outcome according to gestational age at diagnosisF G Sileo, A Kulkarni, I Branescu, et al.
Lancet (London, England)|November 24, 1999
Subtle chromosomal rearrangements in children with unexplained mental retardationS J Knight, R Regan, A Nicod, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|September 27, 2020
A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective reviewE Dempsey, A Haworth, L Ive, et al.
Pageof 3