Results 41 to 50 of about 1,687,960 (109)

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. [PDF]

open access: yesNat Genet, 2017
Shaw ND   +77 more
europepmc   +1 more source

Brief von Josef Steindl an Toshio Ogata

open access: yes
BRIEF VON JOSEF STEINDL AN TOSHIO OGATA Brief von Josef Steindl an Toshio Ogata ([1]
Steindl, Josef
core  

Brief von Josef Steindl an Krishna Bharadwaj

open access: yes
BRIEF VON JOSEF STEINDL AN KRISHNA BHARADWAJ Brief von Josef Steindl an Krishna Bharadwaj ([1]
Steindl, Josef
core   +1 more source

Biallelic variants in GTF3C3 result in an autosomal recessive disorder with intellectual disability. [PDF]

open access: yesGenet Med
De Hayr L   +36 more
europepmc   +1 more source

Brief von Josef Steindl an Manuela Mosca

open access: yes
BRIEF VON JOSEF STEINDL AN MANUELA MOSCA Brief von Josef Steindl an Manuela Mosca ([1]
Steindl, Josef
core  

The AVIATOR registry: the importance of evaluating long-term patient outcomes. [PDF]

open access: yesAnn Cardiothorac Surg, 2019
de Heer F   +8 more
europepmc   +1 more source

A multi-center, open label, single group, observational clinical trial to investigate the effects of training on the administration of Cardioplexol™. [PDF]

open access: yesFront Cardiovasc Med
Tevaearai Stahel HT   +15 more
europepmc   +1 more source

Brief von Josef Steindl an Jerzy Osiatyński

open access: yes
BRIEF VON JOSEF STEINDL AN JERZY OSIATYŃSKI Brief von Josef Steindl an Jerzy Osiatyński (-
Steindl, Josef
core  

Brief von Josef Steindl an Jan Kregel

open access: yes
BRIEF VON JOSEF STEINDL AN JAN KREGEL Brief von Josef Steindl an Jan Kregel ([1]
Steindl, Josef
core   +1 more source

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