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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 13, 2005
Risk of tumorigenesis in overgrowth syndromes: a comprehensive reviewPablo Lapunzina
Biology of the Cell|June 10, 2011
The consequences of uniparental disomy and copy number neutral loss-of-heterozygosity during human development and cancerPablo Lapunzina, David Monk
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 10, 2006
Follow-up and risk of tumors in overgrowth syndromesRicardo Gracia Bouthelier, Pablo Lapunzina
American Journal of Medical Genetics. Part A|September 18, 2008
Capillary malformation of the lower lip, lymphatic malformation of the face and neck, asymmetry and partial/generalized overgrowth (CLAPO): report of six cases of a new syndrome/associationJuan Carlos López-Gutiérrez, Pablo Lapunzina
The Journal of Pediatrics|February 28, 2002
Risks of congenital anomalies in large for gestational age infantsPablo Lapunzina, Jorge S López Camelo, Monica Rittler, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 14, 2008
Umbilical cord stricture is not a genetic anomaly: a study in twinsJosé I Rodríguez, Adrián Mariño-Enríquez, Judith Suárez-Aguado, et al.
American Journal of Medical Genetics. Part A|April 14, 2007
Otopalatodigital syndrome type 2 in two siblings with a novel filamin A 629G>T mutation: clinical, pathological, and molecular findingsAdrián Mariño-Enríquez, Pablo Lapunzina, Stephen P Robertson, et al.
BMC Pediatrics|October 9, 2024
2q31 microdeletion syndrome with the velocardiofacial phenotype and review of the literature: a case reportEstephania Candelo, Sebastian Giraldo-Ocampo, Julian Nevado, et al.
American Journal of Medical Genetics. Part A|September 17, 2008
Laurin-Sandrow syndrome: review and redefinitionAdrián Mariño-Enríquez, Pablo Lapunzina, Félix Omeñaca, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Molecular diagnosis of Beckwith-Wiedemann syndrome using quantitative methylation-sensitive polymerase chain reactionBradford Coffee, Kasinathan Muralidharan, William E Highsmith, et al.
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