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Hallvard Reigstad

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 17, 2021

Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypesSilvia Martin-Almedina, Kazim Ogmen, Ege Sackey, et al.

Frontiers in Pediatrics|July 29, 2021

Extremely Preterm Infant Admissions Within the SafeBoosC-III Consortium During the COVID-19 LockdownMarie Isabel Rasmussen, Mathias Lühr Hansen, Gerhard Pichler, et al.

Nature Genetics|January 10, 2017

De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal developmentChristopher T Gordon, Shifeng Xue, Gökhan Yigit, et al.

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Search research articles

Showing results (21-30 of 23) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 23 results.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 17, 2021

Janus-faced EPHB4-associated disorders: novel pathogenic variants and unreported intrafamilial overlapping phenotypesSilvia Martin-Almedina, Kazim Ogmen, Ege Sackey, et al.

Frontiers in Pediatrics|July 29, 2021

Extremely Preterm Infant Admissions Within the SafeBoosC-III Consortium During the COVID-19 LockdownMarie Isabel Rasmussen, Mathias Lühr Hansen, Gerhard Pichler, et al.

Nature Genetics|January 10, 2017

De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal developmentChristopher T Gordon, Shifeng Xue, Gökhan Yigit, et al.

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