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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Caroline Joyce

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Clinical Case Reports|October 29, 2015

The value of in vitro studies in a case of neonatal diabetes with a novel Kir6.2-W68G mutationSusan M O'Connell, Peter Proks, Holger Kramer, et al.

Laboratory Investigation; a Journal of Technical Methods and Pathology|September 29, 2020

Assessing the utility of long-read nanopore sequencing for rapid and efficient characterization of mobile element insertionsChristopher M Watson, Laura A Crinnion, Helen Lindsay, et al.

Virchows Archiv : an International Journal of Pathology|October 19, 2023

Practical guidelines of the EOTTD for pathological and genetic diagnosis of hydatidiform molesCarla Bartosch, Alfons Nadal, Ana C Braga, et al.

American Journal of Human Genetics|December 4, 2018

DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable ImmunodeficiencyClare V Logan, Jennie E Murray, David A Parry, et al.

Nature Genetics|August 13, 2021

Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopauseJunhua Zhou, Elena A B Azizan, Claudia P Cabrera, et al.

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Search research articles

Showing results (21-30 of 25) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 25 results.

Clinical Case Reports|October 29, 2015

The value of in vitro studies in a case of neonatal diabetes with a novel Kir6.2-W68G mutationSusan M O'Connell, Peter Proks, Holger Kramer, et al.

Laboratory Investigation; a Journal of Technical Methods and Pathology|September 29, 2020

Assessing the utility of long-read nanopore sequencing for rapid and efficient characterization of mobile element insertionsChristopher M Watson, Laura A Crinnion, Helen Lindsay, et al.

Virchows Archiv : an International Journal of Pathology|October 19, 2023

Practical guidelines of the EOTTD for pathological and genetic diagnosis of hydatidiform molesCarla Bartosch, Alfons Nadal, Ana C Braga, et al.

American Journal of Human Genetics|December 4, 2018

DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable ImmunodeficiencyClare V Logan, Jennie E Murray, David A Parry, et al.

Nature Genetics|August 13, 2021

Somatic mutations of GNA11 and GNAQ in CTNNB1-mutant aldosterone-producing adenomas presenting in puberty, pregnancy or menopauseJunhua Zhou, Elena A B Azizan, Claudia P Cabrera, et al.

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