Results 171 to 180 of about 83,600 (245)

A New Case of Nager Syndrome as a Rare Cause of Acrofacial Dysostosis. [PDF]

Mol Syndromol
Aglamis Senel O, Kilic E.
europepmc   +1 more source

Enhancement of laryngeal contrasts in non-native English clear speech: a comparison between L2-immersed sequential bilinguals and L1-immersed speakers. [PDF]

Front Hum Neurosci
Jung YJ, Dmitrieva O.
europepmc   +1 more source

Unmasking Guion-Almeida syndrome: clinical and genetic insights from a 3-year-old with EFTUD2 mutation

Linda Jacob, Jewel M. George, Carol S. Cherian, Jacob Abraham   +3 more
openalex   +2 more sources

Low-Set Ears: A New Marker of Fetal Chromosomal Anomalies. [PDF]

Fetal Diagn Ther
Baldrich-Martin E, Jalencas G, Mazano I, Lesmes-Heredia C, Manresa-Dominguez JM, Iniguez-Cruz M, Ferreres JC, Beltran V, Borrell A.   +8 more
europepmc   +1 more source

Guion. Nociones sobre la escritura audiovisual

, 2014
Pedro Javier Gómez Martínez
openalex   +1 more source

WAWAI WADA KIDODE : uso de elementos y estructuras narrativas indígenas del Caribe y la Amazonía para crear un guion de novela gráfica y otros artefactos narrativos fractales

, 2020
Máncel Enrique Martínez Ramos
openalex   +1 more source

Perfil de puesto para vendedor de piso: guion de entrevista

, 2017
A. I. Castelán-Olivares, A. Martín-Tovar, D. Barrera-Trejo, S. L. Ascencio-Sánchez, M. L. Bautista-Díaz   +4 more
openalex   +1 more source

Proteogenomic characterization of invasive breast tumors in young women. [PDF]

NPJ Breast Cancer
Raj-Kumar PK, Liu J, Soltis AR, Bateman NW, Chen Q, Sturtz LA, Deyarmin B, Pierobon M, Abulez TA, Praveen-Kumar A, Zhang X, Nguyen T, Yan C, Hu Y, Guion K, Hooke JA, Kovatich AJ, Fantacone-Campbell L, Mostoller B, Kvecher L, Somiari S, Steeg PS, Rajagopal PS, Darcy KM, Lee JSH, Dalgard CL, Conrads TP, Petricoin EF, Meerzaman D, Wilkerson MD, APOLLO Research Network, Lin X, Shriver CD, Lipkowitz S, Hu H.   +34 more
europepmc   +1 more source

A novel <i>EFTUD2</i> splicing variant causing mandibulofacial dysostosis with microcephaly: a case report. [PDF]

Transl Pediatr
Xu Y, Zhang X, Lu W, Xiao Y, Ma X, Chen L, Dong Z.   +6 more
europepmc   +1 more source

A Candidate Gene for Cerebro-Oculo-Nasal Syndrome: A Zinc-Finger Gene <i>ZNF185</i> Located at Xq28. [PDF]

Mol Syndromol
Hazan F, Yılmaz Uzman C, Emecen DA, Yılmazer MM, Öztürk T, Bilen MM, Hüvez A, İlhan R, Genel F, Ballar P.   +9 more
europepmc   +1 more source