Results 211 to 220 of about 4,732,768 (360)
Francisco Pizarro (1478?-1541), figura central de la Conquista española, como Cortés en México, entró tardíamente en la Historia, cuando a más de cincuenta años descubrió el Perú y sus fabulosas riquezas. Hijo bastardo de un militar hidalgo adinerado y de una criada, Pizarro nació y se crió pobre en Estremadura y fue analfabeto toda su vida. Muy joven,
openaire +1 more source
United States Department of Health and Human Services. Centers for Disease Control and Prevention +1 more
openalex +1 more source
ABSTRACT There is a strong genetic contribution to the etiology of congenital diaphragmatic hernia (CDH). This study evaluated genetic testing results and diagnostic yield for fetuses and children with CDH. This was a retrospective cohort study of exome sequencing (ES) performed at GeneDx for fetuses and children ≤ 18 years of age with CDH compared ...
Justin Blair +9 more
wiley +1 more source
Correction: Circadian system functional status and sleep in blind subjects with and without conscious light perception. [PDF]
Martínez-Martínez D +5 more
europepmc +1 more source
The aim of this paper is to analyze the story "El mico", by Francisco Tario, a Hispanic-Mexican writer. First, I will make the overall presentation of an author and a work little-known outside of Mexican literature. Second, the analysis will highlight the problem that, in fantasy literature,the limits of language as an instrument of representation are ...
openaire +2 more sources
Design of the containment reservoir in the Lonqueador River basin to flooding mitigation in the Francisco Beltrão urban area [PDF]
Camila Daiane Cancelier Steinhorst
openalex
Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet +10 more
wiley +1 more source
Author Correction: Myocardial reprogramming by HMGN1 underlies heart defects in trisomy 21. [PDF]
Ranade SS +22 more
europepmc +1 more source

