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1.
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder.
Am J Med Genet A
; 185(8): 2384-2390, 2021 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34003604
2.
Conditions requiring hospitalisations, more than general anaesthesia itself, are associated with diagnosis of learning disorders in children.
Anaesth Crit Care Pain Med
; 39(6): 777-783, 2020 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-32977071
3.
De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature.
Eur J Hum Genet
; 28(6): 770-782, 2020 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-32005960
4.
ERP variabilities as a function of reading maturation.
Neurophysiol Clin
; 46(4-5): 313-315, 2016 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-26899932
5.
Obstetrical and neonatal characteristics vary with birthweight in a cohort of 100 term newborns with symptomatic arterial ischemic stroke.
Eur J Paediatr Neurol
; 14(3): 206-13, 2010 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-19541515
6.
Delayed language development at two years of age in very preterm infants in the Perinatal Network of Haute-Normandie.
Early Hum Dev
; 90(12): 891-2, 2014 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-25463837
7.
Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase.
J Biol Chem
; 277(28): 25815-22, 2002 Jul 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-11983712
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