ZELULA AMAK ETA TERAPIA ZELULARRA
University of Groningen
Groninga, HolandaUniversity of Groningen-ko ikertzaileekin lankidetzan egindako argitalpenak (12)
2020
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Primrose syndrome: Characterization of the phenotype in 42 patients
Clinical Genetics, Vol. 97, Núm. 6, pp. 890-901
2019
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Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome (Genetics in Medicine, (2019), 21, 6, (1295-1307), 10.1038/s41436-018-0330-z)
Genetics in Medicine
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The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome
Genetics in Medicine, Vol. 21, Núm. 6, pp. 1295-1307
2018
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Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features
American Journal of Human Genetics, Vol. 103, Núm. 5, pp. 786-793
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The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants [version 1; referees: 3 approved]
Wellcome Open Research, Vol. 3
2013
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Phenotypic spectrum and prevalence of INPP5E mutations in Joubert Syndrome and related disorders
European Journal of Human Genetics, Vol. 21, Núm. 10, pp. 1074-1078
2007
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Survival and health in liveborn infants with transposition of great arteries - A population-based study
Congenital Heart Disease, Vol. 2, Núm. 3, pp. 165-169
2006
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Erratum: Preventing neural tube defects in Europe: A missed opportunity (Reproductive Toxicology (2005) 20 (393-402) DOI: 10.1016/j.reprotox.2005.03. 009)
Reproductive Toxicology
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The potential of the European network of congenital anomaly registers (EUROCAT) for drug safety surveillance: A descriptive study
Pharmacoepidemiology and Drug Safety, Vol. 15, Núm. 9, pp. 675-682
2005
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Preventing neural tube defects in Europe: A missed opportunity
Reproductive Toxicology, Vol. 20, Núm. 3, pp. 393-402
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Trends and geographic inequalities in the prevalence of Down syndrome in Europe, 1980-1999
Revue d'Epidemiologie et de Sante Publique
2004
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Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe
Prenatal Diagnosis, Vol. 24, Núm. 11, pp. 908-912