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Orphanet Journal of Rare Diseases|August 17, 2019
Correction to: Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare diseaseLibby Wood, Guillaume Bassez, Corinne Bleyenheuft, et al.
Human Molecular Genetics|January 9, 2013
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of FallotHeather J Cordell, Ana Töpf, Chrysovalanto Mamasoula, et al.
Maturitas|April 22, 2025
No increased arterial stiffness after premenopausal risk-reducing salpingo-oophorectomy (RRSO)Maarten J Beekman, Lara Terra, Jeanine E Roeters van Lennep, et al.
Nature Genetics|November 13, 2012
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2Richard J L F Lemmers, Rabi Tawil, Lisa M Petek, et al.
Maturitas|February 22, 2026
Long-term outcomes of surgical menopause after risk-reducing salpingo-oophorectomy: results of the HARMOny studyMaarten J Beekman, Lara Terra, Eveline M A Bleiker, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|July 3, 2023
Urinary incontinence more than 15 years after premenopausal risk-reducing salpingo-oophorectomy: a multicentre cross-sectional studyLara Terra, Bernadette A M Heemskerk-Gerritsen, Maarten J Beekman, et al.
Physical Review Letters|May 1, 2026
Test of the Gravitational Force Law on Cosmological Scales Using the Kinematic Sunyaev-Zeldovich EffectP A Gallardo, K Pardo, O H E Philcox, et al.
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