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Showing results (151-160 of 157) with videos related to

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Journal of Medical Genetics|January 3, 2001
A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 casesP de Lonlay, N Seta, S Barrot, et al.
Breast Cancer Research and Treatment|February 29, 2012
Evaluation of RAD51C as cancer susceptibility gene in a large breast-ovarian cancer patient population referred for genetic testingK De Leeneer, M Van Bockstal, S De Brouwer, et al.
Human Molecular Genetics|September 5, 2001
The mutational spectrum of human malignant autosomal recessive osteopetrosisC Sobacchi, A Frattini, P Orchard, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
The Lancet. Gastroenterology & Hepatology|August 21, 2018
Endoscopic versus percutaneous biliary drainage in patients with resectable perihilar cholangiocarcinoma: a multicentre, randomised controlled trialRobert J S Coelen, Eva Roos, Jimme K Wiggers, et al.
Blood|September 15, 1995
Factor VIII gene inversions in severe hemophilia A: results of an international consortium studyS E Antonarakis, J P Rossiter, M Young, et al.
Cancers|July 9, 2020
Resectability and Ablatability Criteria for the Treatment of Liver Only Colorectal Metastases: Multidisciplinary Consensus Document from the COLLISION Trial GroupSanne Nieuwenhuizen, Robbert S Puijk, Bente van den Bemd, et al.
Pageof 16

Showing results (151-160 of 157) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 157 results.
Journal of Medical Genetics|January 3, 2001
A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 casesP de Lonlay, N Seta, S Barrot, et al.
Breast Cancer Research and Treatment|February 29, 2012
Evaluation of RAD51C as cancer susceptibility gene in a large breast-ovarian cancer patient population referred for genetic testingK De Leeneer, M Van Bockstal, S De Brouwer, et al.
Human Molecular Genetics|September 5, 2001
The mutational spectrum of human malignant autosomal recessive osteopetrosisC Sobacchi, A Frattini, P Orchard, et al.
American Journal of Human Genetics|June 23, 1998
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosisK Buiting, B Dittrich, S Gross, et al.
The Lancet. Gastroenterology & Hepatology|August 21, 2018
Endoscopic versus percutaneous biliary drainage in patients with resectable perihilar cholangiocarcinoma: a multicentre, randomised controlled trialRobert J S Coelen, Eva Roos, Jimme K Wiggers, et al.
Blood|September 15, 1995
Factor VIII gene inversions in severe hemophilia A: results of an international consortium studyS E Antonarakis, J P Rossiter, M Young, et al.
Cancers|July 9, 2020
Resectability and Ablatability Criteria for the Treatment of Liver Only Colorectal Metastases: Multidisciplinary Consensus Document from the COLLISION Trial GroupSanne Nieuwenhuizen, Robbert S Puijk, Bente van den Bemd, et al.
Pageof 16