Results 211 to 220 of about 4,732,768 (360)

Francisco Pizarro

open access: yes, 2004
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

Percentage of Adults Who Report Driving After Drinking Too Much (in the past 30 days), 2012 & 2014, Region 9 - San Francisco

open access: green
United States Department of Health and Human Services. Centers for Disease Control and Prevention   +1 more
openalex   +1 more source

Genomic Contributors to Congenital Diaphragmatic Hernia: Results of Exome Sequencing in 560 Probands and Cross Reference of Findings in an Independent Cohort

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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]

open access: yesFront Physiol
Martínez-Martínez D   +5 more
europepmc   +1 more source

Francisco Tari

open access: yes, 2016
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

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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]

open access: yesNature
Ranade SS   +22 more
europepmc   +1 more source

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