Results 141 to 150 of about 59,149 (243)

Human Development and Reconsideration of Ensoulment [PDF]

, 1993
Kischer, Clayton Ward
core   +1 more source

Comprehensive assessment of whole-genome sequencing-based variant calling pipelines in monozygotic twins. [PDF]

Brief Bioinform
Tan C, Sun W, Yu J, Fu J, Ming C, Liu X.
europepmc   +1 more source

Concurrent uveitis in monozygotic twins in the context of systemic sarcoidosis. [PDF]

J Ophthalmic Inflamm Infect
Ashour DM, Mohsen R, Elziaty RA, Attia OB, Diab HS, Tawfik CA.   +5 more
europepmc   +1 more source

Genetic impacts on within-pair DNA methylation variance in monozygotic twins capture gene-environment interactions and cell-type effects. [PDF]

Genome Biol
Zhang X, Yet I, Villicaña S, Castillo-Fernandez J, Mangino M, Hottenga JJ, Tsai PC, Min JL, Falchi M, Wong A, Boomsma DI, Ong KK, van Dongen J, Bell JT.   +13 more
europepmc   +1 more source

Clinical differences in monozygotic twins with Rett syndrome: case report and systematic review. [PDF]

Orphanet J Rare Dis
Boeri S, Piai M, Russo S, Alari V, Cogliati F, Simonetta D, Benke TA, Nobili L, Prato G.   +8 more
europepmc   +1 more source

Functional Movement Disorder in Familial Ataxia: A Case Report of Monozygotic Twins. [PDF]

Mov Disord Clin Pract
Kern D, Windpassinger C, Schwingenschuh P.   +2 more
europepmc   +1 more source

Monozygotic twins affected by SAPHO syndrome. [PDF]

An Bras Dermatol
Scandagli I, Rosi E, Silvi G, Ruggieri M, Amadori T, Prignano F.   +5 more
europepmc   +1 more source

A multi-omics study on monozygotic twins discordant for amyotrophic lateral sclerosis and literature review underline a potential role for innate immunity and epigenetic dysregulation in disease mechanisms. [PDF]

Neurol Sci
Tosi M, Favero F, Zuccalà M, Visha E, Caushi F, Barizzone N, Pomella N, Follia L, Corrado L, Corà D, Martignetti L, Leone M, D'Alfonso S.   +12 more
europepmc   +1 more source

Genetics of monozygotic twins reveals the impact of environmental sensitivity on psychiatric and neurodevelopmental phenotypes. [PDF]

Nat Hum Behav
Assary E, Coleman JRI, Hemani G, van de Weijer MP, Howe LJ, Palviainen T, Grasby KL, Ahlskog R, Nygaard M, Cheesman R, Lim K, Reynolds CA, Ordoñana JR, Colodro-Conde L, Gordon S, Madrid-Valero JJ, Thalamuthu A, Hottenga JJ, Mengel-From J, Armstrong NJ, Sachdev PS, Lee T, Brodaty H, Trollor JN, Wright M, Ames D, Catts VS, Latvala A, Within Family Consortium, Vuoksimaa E, Mallard T, Paige Harden K, Tucker-Drob EM, Oskarsson S, Hammond CJ, Christensen K, Taylor M, Lundström S, Larsson H, Karlsson R, Pedersen NL, Mather KA, Medland SE, Boomsma DI, Martin NG, Plomin R, Bartels M, Lichtenstein P, Kaprio J, Eley TC, Davies NM, Munroe PB, Keers R.   +52 more
europepmc   +1 more source

Concordant X-linked hypophosphatemic rickets in monozygotic twins: diagnostic challenges and a novel genetic insight. [PDF]

Endocrinol Diabetes Metab Case Rep
Ribeiro S, Moreno T, Varela A, Soares G, Queirós J.   +4 more
europepmc   +1 more source