Results 161 to 170 of about 20,549 (261)

CRISPR-Cas9-Generated TXNDC15 c.560delA Homozygous Mouse Model Exhibits Meckel-Gruber Syndrome Phenotype. [PDF]

Genesis
Liu Y, Wang H, Chen L, Wu X, Xu Z, Huang Q, Zhang H, Cao X, Liang X, Zhong X, Luo C.   +10 more
europepmc   +1 more source

Atypical Retinitis Pigmentosa With Systemic Features in Bardet-Biedl Syndrome. [PDF]

Clin Case Rep
Ahsan MU, Shaheen S, Ahmed S.
europepmc   +1 more source

Polydactyly

, 2010
Yuranga Weerakkody, Mohammad Taghi Niknejad, Joshua Yap   +2 more
openaire   +2 more sources

Central Ray Synpolydactyly with Bilateral Medial Foot Polydactyly and Hydrocephalus: A Case Report. [PDF]

Plast Reconstr Surg Glob Open
Alobaidi H, Suraya F, Alrajhi R, Alghamdi AM, Mirza M.   +4 more
europepmc   +1 more source

Non-Crosslinked Hyaluronic Acid Redensity 1^® Supports Cell Viability, Proliferation, and Collagen Deposition in Early Burn Management. [PDF]

Pharmaceutics
Liao Z, Chen X, Brusini R, Faivre J, Applegate LA, Flegeau K, Hirt-Burri N.   +6 more
europepmc   +1 more source

A Rare Foot Duplication; Mirror Foot - Case Report. [PDF]

Sisli Etfal Hastan Tip Bul
Akpinar I, Cerikan MD, Dilek OF.
europepmc   +1 more source

Detection of the Heterozygous Recurrent MAX p.(Arg60Gln) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly-Macrocephaly Syndrome. [PDF]

Clin Genet
Showpnil IA, Feinstein-Goren N, Greenbaum L, Barel O, Koboldt DC, Brugmann SA, Weaver KN, Slavotinek A, Pode-Shakked B, Stottmann RW.   +9 more
europepmc   +1 more source

A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family. [PDF]

Genet Mol Biol
Fatima S, Sun D, Han J, Qiu M, Ahmad S, Zubair M, Ali MZ, Abbas S, Shafiq M, Muzammal M, Gul H, Khan J, Du S, Khan MA.   +13 more
europepmc   +1 more source