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The Journal of Clinical Endocrinology and Metabolism|September 24, 1998
Molecular analysis of the ret and GDNF genes in a family with multiple endocrine neoplasia type 2A and Hirschsprung diseaseS Borrego, C Eng, B Sánchez, et al.Clinical Genetics|June 1, 1992
Familial spastic paraplegia with neuropathy and poikiloderma. A new syndrome?G Antiñolo, M Nieto, S Borrego, et al.Molecular Human Reproduction|February 26, 2004
Analysis of the involvement of CCR5-Delta32 and CCR2-V64I variants in the development of endometriosisG Antiñolo, R M Fernández, J A Noval, et al.Journal of Medical Genetics|June 27, 2009
Contribution of RET, NTRK3 and EDN3 to the expression of Hirschsprung disease in a multiplex familyA Sánchez-Mejías, R M Fernández, M López-Alonso, et al.Clinical Endocrinology|October 9, 2001
Germline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish populationA Ruiz, G Antiñolo, R M Fernández, et al.Anales Espanoles De Pediatria|August 1, 1988
[Study of isochromosomes of the long arms of the X chromosome]S Borrego, C Fernández-Novoa, V San Martín, et al.Anales Espanoles De Pediatria|September 1, 1988
[Roberts-SC phocomelia syndrome: cytogenetic findings and clinical variability in three brothers]G Antiñolo Gil, S Borrego López, M Cañadas García de León, et al.Developmental Biology|June 21, 2016
Epigenetics in ENS development and Hirschsprung diseaseA Torroglosa, M M Alves, R M Fernández, et al.Journal of Medical Genetics|October 21, 1999
Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expressionS Borrego, M E Sáez, A Ruiz, et al.Ophthalmic Genetics|September 1, 1996
G106R rhodopsin mutation is also present in Spanish ADRP patientsC Ayuso, C Reig, B Garcia-Sandoval, et al.Pageof 4