E. Galán-Gómez

Intrauterine growth retardation, duodenal and extrahepatic biliary atresia, hypoplastic pancreas and other intestinal anomalies: further evidence of the Martínez-Frías syndrome.

E. Galán-Gómez, E. B. Sánchez, S. Arias-Castro, 2007, European journal of medical genetics.

Early response to idursulfase treatment in a 3 year-old boy affected of Hunter syndrome.

E. Galán-Gómez, J. Cardesa-García, C. Cáceres-Marzal, 2008, European journal of medical genetics.

Unrelated chromosomal anomalies found in patients with suspected 22q11.2 deletion

D. Heine-Suñer, P. Lapunzina, J. Rosell, 2008, American journal of medical genetics. Part A.

Clinical manifestations in female carriers of mucopolysaccharidosis type II: a spanish cross-sectional study

M. Couce, E. Galán-Gómez, E. Guillén-Navarro, 2013, Orphanet Journal of Rare Diseases.

Schuurs–Hoeijmakers Syndrome (PACS1 Neurodevelopmental Disorder): Seven Novel Patients and a Review

Á. Carracedo, L. Pérez-Jurado, P. Lapunzina, 2021, Genes.

Waardenburg syndrome type 4: Report of two new cases caused by SOX10 mutations in Spain

S. Borrego, G. Antiñolo, R. Fernández, 2014, American journal of medical genetics. Part A.

A Scoring System to Predict the Severity of Hirschsprung Disease at Diagnosis and Its Correlation With Molecular Genetics

S. Borrego, E. Galán-Gómez, J. Ruiz-Contreras, 2016, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Tracheoesophageal anomalies in oculoauriculovertebral (Goldenhar) spectrum

R. Sutphen, B. Kousseff, E. Galán-Gómez, 1995, Clinical genetics.