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Showing results (11-20 of 14) with videos related to

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Cancer Causes & Control : CCC|November 8, 2002
Obesity, body size, and risk of postmenopausal breast cancer: the Women's Health Initiative (United States)Libby M Morimoto, Emily White, Z Chen, et al.
British Journal of Cancer|March 18, 2004
Loss of heterozygosity on 10q and mutational status of PTEN and BMPR1A in colorectal primary tumours and metastasesM Karoui, C Tresallet, C Julie, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 14, 2017
Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter studyM Egloff, B Hervé, T Quibel, et al.
American Journal of Human Genetics|August 19, 2007
Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international studyL Faivre, G Collod-Beroud, B L Loeys, et al.
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Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Cancer Causes & Control : CCC|November 8, 2002
Obesity, body size, and risk of postmenopausal breast cancer: the Women's Health Initiative (United States)Libby M Morimoto, Emily White, Z Chen, et al.
British Journal of Cancer|March 18, 2004
Loss of heterozygosity on 10q and mutational status of PTEN and BMPR1A in colorectal primary tumours and metastasesM Karoui, C Tresallet, C Julie, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 14, 2017
Diagnostic yield of chromosomal microarray analysis in fetuses with isolated increased nuchal translucency: a French multicenter studyM Egloff, B Hervé, T Quibel, et al.
American Journal of Human Genetics|August 19, 2007
Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international studyL Faivre, G Collod-Beroud, B L Loeys, et al.
Pageof 2