BLANCA
GENER QUEROL
Hospital del Mar
Barcelona, EspañaHospital del Mar -ko ikertzaileekin lankidetzan egindako argitalpenak (4)
2022
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FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects
Genetics in Medicine, Vol. 24, Núm. 12, pp. 2475-2486
2015
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Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders
Molecular Autism, Vol. 6, Núm. 1
2014
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Pseudohypoparathyroidism vs. tricho-rhino-phalangeal syndrome: Patient reclassification
Journal of Pediatric Endocrinology and Metabolism, Vol. 27, Núm. 11-12, pp. 1089-1094
2007
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Small supernumerary marker chromosome causing partial trisomy 6p in a child with craniosynostosis
American Journal of Medical Genetics, Part A, Vol. 143, Núm. 10, pp. 1108-1113