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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 1
1988 1
1989 3
1990 1
1991 1
1993 2
1995 4
1998 2
2001 1
2004 4
2006 1
2007 2
2008 3
2010 3
2012 2
2013 5
2014 2
2017 2
2018 1
2019 1
2021 4
2024 0

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42 results

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Page 1
Clitoromegaly in neurofibromatosis.
Sutphen R, Galán-Goméz E, Kousseff BG. Sutphen R, et al. Among authors: galan gomez e. Am J Med Genet. 1995 Jan 30;55(3):325-30. doi: 10.1002/ajmg.1320550316. Am J Med Genet. 1995. PMID: 7726231 Review.
Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications.
Perea-Romero I, Gordo G, Iancu IF, Del Pozo-Valero M, Almoguera B, Blanco-Kelly F, Carreño E, Jimenez-Rolando B, Lopez-Rodriguez R, Lorda-Sanchez I, Martin-Merida I, Pérez de Ayala L, Riveiro-Alvarez R, Rodriguez-Pinilla E, Tahsin-Swafiri S, Trujillo-Tiebas MJ; ESRETNET Study Group; ERDC Study Group; Associated Clinical Study Group; Garcia-Sandoval B, Minguez P, Avila-Fernandez A, Corton M, Ayuso C. Perea-Romero I, et al. Sci Rep. 2021 Jan 15;11(1):1526. doi: 10.1038/s41598-021-81093-y. Sci Rep. 2021. PMID: 33452396 Free PMC article.
[Holt-Oram syndrome].
Cáceres Marzal C, Galán Gómez E, Campo Sampedro FM, Cardesa García JJ. Cáceres Marzal C, et al. Among authors: galan gomez e. An Pediatr (Barc). 2004 Jan;60(1):91-2. doi: 10.1016/s1695-4033(04)78225-9. An Pediatr (Barc). 2004. PMID: 14718140 Free article. Spanish. No abstract available.
Complications related to Turner syndrome.
Bejarano Ramírez N, Redondo Calvo FJ, Galán Gómez E. Bejarano Ramírez N, et al. Among authors: galan gomez e. Med Clin (Barc). 2017 Jul 7;149(1):39-40. doi: 10.1016/j.medcli.2017.02.016. Epub 2017 Apr 4. Med Clin (Barc). 2017. PMID: 28389010 English, Spanish. No abstract available.
Kabuki make-up (Niikawa-Kuroki) syndrome in five Spanish children.
Galán-Gómez E, Cardesa-García JJ, Campo-Sampedro FM, Salamanca-Maesso C, Martínez-Frías ML, Frías JL. Galán-Gómez E, et al. Am J Med Genet. 1995 Nov 20;59(3):276-82. doi: 10.1002/ajmg.1320590303. Am J Med Genet. 1995. PMID: 8599349 Review.
Schuurs-Hoeijmakers Syndrome (PACS1 Neurodevelopmental Disorder): Seven Novel Patients and a Review.
Tenorio-Castaño J, Morte B, Nevado J, Martinez-Glez V, Santos-Simarro F, García-Miñaúr S, Palomares-Bralo M, Pacio-Míguez M, Gómez B, Arias P, Alcochea A, Carrión J, Arias P, Almoguera B, López-Grondona F, Lorda-Sanchez I, Galán-Gómez E, Valenzuela I, Méndez Perez MP, Cuscó I, Barros F, Pié J, Ramos S, Ramos FJ, Kuechler A, Tizzano E, Ayuso C, Kaiser FJ, Pérez-Jurado LA, Carracedo Á, The ENoD-Ciberer Consortium, The Side Consortium, Lapunzina P. Tenorio-Castaño J, et al. Among authors: galan gomez e. Genes (Basel). 2021 May 13;12(5):738. doi: 10.3390/genes12050738. Genes (Basel). 2021. PMID: 34068396 Free PMC article.
A new overgrowth syndrome is due to mutations in RNF125.
Tenorio J, Mansilla A, Valencia M, Martínez-Glez V, Romanelli V, Arias P, Castrejón N, Poletta F, Guillén-Navarro E, Gordo G, Mansilla E, García-Santiago F, González-Casado I, Vallespín E, Palomares M, Mori MA, Santos-Simarro F, García-Miñaur S, Fernández L, Mena R, Benito-Sanz S, del Pozo Á, Silla JC, Ibañez K, López-Granados E, Martín-Trujillo A, Montaner D; SOGRI Consortium; Heath KE, Campos-Barros Á, Dopazo J, Nevado J, Monk D, Ruiz-Pérez VL, Lapunzina P. Tenorio J, et al. Hum Mutat. 2014 Dec;35(12):1436-41. doi: 10.1002/humu.22689. Hum Mutat. 2014. PMID: 25196541
42 results