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J Willems

Showing results (431-440 of 446) with videos related to

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American Journal of Medical Genetics. Part A|August 16, 2012
Phenotypic variability of atypical 22q11.2 deletions not including TBX1Judith M A Verhagen, Karin E M Diderich, Grétel Oudesluijs, et al.
Acta Cardiologica|January 1, 1978
Antihypertensive therapy in patients above age 60. Third interim report of the European Working Party on High blood pressure in Elderly (EWPHE)A Amery, P Berthaux, W Birkenhäger, et al.
European Journal of Pediatrics|January 29, 2013
Paediatric community-acquired septic shock: results from the REPEM network studyP Van de Voorde, B Emerson, B Gomez, et al.
Human Genetics|October 17, 2007
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6pMarja W Wessels, Bianca M De Graaf, Titia E Cohen-Overbeek, et al.
Human Molecular Genetics|October 1, 1996
Positional cloning of a gene involved in hereditary multiple exostosesW Wuyts, W Van Hul, J Wauters, et al.
The Journal of Allergy and Clinical Immunology|May 28, 2021
Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXASCaspar I van der Made, Judith Potjewijd, Annemiek Hoogstins, et al.
American Journal of Human Genetics|June 30, 2009
Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsyAnnemieke J M H Verkerk, Rachel Schot, Belinda Dumee, et al.
European Journal of Human Genetics : EJHG|April 17, 2014
The SMAD-binding domain of SKI: a hotspot for de novo mutations causing Shprintzen-Goldberg syndromeDorien Schepers, Alexander J Doyle, Gretchen Oswald, et al.
Nature Plants|January 15, 2020
Reciprocal cybrids reveal how organellar genomes affect plant phenotypesPádraic J Flood, Tom P J M Theeuwen, Korbinian Schneeberger, et al.
Human Mutation|March 17, 2010
Mucopolysaccharidosis type IIID: 12 new patients and 15 novel mutationsMarlies J Valstar, Aida M Bertoli-Avella, Marja W Wessels, et al.
Pageof 45

Showing results (431-440 of 446) with videos related to

Sort By:
Pageof 45
American Journal of Medical Genetics. Part A|August 16, 2012
Phenotypic variability of atypical 22q11.2 deletions not including TBX1Judith M A Verhagen, Karin E M Diderich, Grétel Oudesluijs, et al.
Acta Cardiologica|January 1, 1978
Antihypertensive therapy in patients above age 60. Third interim report of the European Working Party on High blood pressure in Elderly (EWPHE)A Amery, P Berthaux, W Birkenhäger, et al.
European Journal of Pediatrics|January 29, 2013
Paediatric community-acquired septic shock: results from the REPEM network studyP Van de Voorde, B Emerson, B Gomez, et al.
Human Genetics|October 17, 2007
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6pMarja W Wessels, Bianca M De Graaf, Titia E Cohen-Overbeek, et al.
Human Molecular Genetics|October 1, 1996
Positional cloning of a gene involved in hereditary multiple exostosesW Wuyts, W Van Hul, J Wauters, et al.
The Journal of Allergy and Clinical Immunology|May 28, 2021
Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXASCaspar I van der Made, Judith Potjewijd, Annemiek Hoogstins, et al.
American Journal of Human Genetics|June 30, 2009
Mutation in the AP4M1 gene provides a model for neuroaxonal injury in cerebral palsyAnnemieke J M H Verkerk, Rachel Schot, Belinda Dumee, et al.
European Journal of Human Genetics : EJHG|April 17, 2014
The SMAD-binding domain of SKI: a hotspot for de novo mutations causing Shprintzen-Goldberg syndromeDorien Schepers, Alexander J Doyle, Gretchen Oswald, et al.
Nature Plants|January 15, 2020
Reciprocal cybrids reveal how organellar genomes affect plant phenotypesPádraic J Flood, Tom P J M Theeuwen, Korbinian Schneeberger, et al.
Human Mutation|March 17, 2010
Mucopolysaccharidosis type IIID: 12 new patients and 15 novel mutationsMarlies J Valstar, Aida M Bertoli-Avella, Marja W Wessels, et al.
Pageof 45