Anencephaly and faciocranioschisis : Evidence of complete failure of closure 3 of the neural tube in humansURIOSTE, M; ROSA, A.American journal of medical genetics. 1998, Vol 75, Num 1, pp 4-6, issn 0148-7299Article

DNA copy number profiling reveals extensive genomic loss in hereditary BRCA1 and BRCA2 ovarian carcinomasKAMIENIAK, M. M; MUNOZ-REPETO, I; SAEZ, R et al.British journal of cancer. 2013, Vol 108, Num 8, pp 1732-1742, issn 0007-0920, 11 p.Article

Clinical/epidemiological analysis of congenital anomalies associated with diaphragmatic herniaMARTINEZ-FRIAS, M.-L; PRIETO, L; URIOSTE, M et al.American journal of medical genetics. 1996, Vol 62, Num 1, pp 71-76, issn 0148-7299Article

Sclerocornea, hyperterolism, syndactyly, and ambiguous genitaliaMARTINEZ-FRIAS, M. L; BERMEJO, E; SANCHEZ OTERO, T et al.American journal of medical genetics. 1994, Vol 49, Num 2, pp 195-197, issn 0148-7299Article

Complex cytogenetic abnormalities including telomeric associations and MEN1 mutation in a pediatric ependymomaURIOSTE, M; MARTINEZ-RAMIREZ, A; CIGUDOSA, J. C et al.Cancer genetics and cytogenetics. 2002, Vol 138, Num 2, pp 107-110, issn 0165-4608, 4 p.Article

Chromosomal changes pattern and gene amplification in T cell non-Hodgkin's lymphomasRENEDO, M; MARTINEZ-DELGADO, B; ARRANZ, E et al.Leukemia. 2001, Vol 15, Num 10, pp 1627-1632, issn 0887-6924Article

Persistence of müllerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly, renal and craniofacial anomaliesURIOSTE, M; RODRIGUEZ, J. I; BARCIA, J. M et al.American journal of medical genetics. 1993, Vol 47, Num 4, pp 494-503, issn 0148-7299Article

Diploid/tetraploid mosaicism in a stillborn infant with prune belly anomalyURIOSTE, M; PINEL, I; GOMAR, J. L et al.Annales de génétique (Paris). 1990, Vol 33, Num 1, pp 49-51, issn 0003-3995Article

Giant-cell chondrodysplasia in a male infant with clinical and radiological findings resembling the Piepkorn type of lethal osteochondrodysplasiaURIOSTE, M; RODRIGUEZ, J. I; BOFARULL, J. M et al.American journal of medical genetics. 1997, Vol 68, Num 3, pp 342-346, issn 0148-7299Conference Paper

Dynamic mosaicism involving an unstable supernumerary der(22) chromosome in cat eye syndromeURIOSTE, M; VISEDO, G; SANCHIS, A et al.American journal of medical genetics. 1994, Vol 49, Num 1, pp 77-82, issn 0148-7299Article

Methimazole in animal feed and congenital aplasia cutisMARTINEZ-FRIAS, M. L; CEREIJO, A; RODRIGUEZ-PINILLA, E et al.Lancet (British edition). 1992, Vol 339, Num 8795, pp 742-743, issn 0140-6736Article

New acrofacial dysostosis syndrome in 3 sibsRODRIGUEZ, J. I; PALACIOS, J; URIOSTE, M et al.American journal of medical genetics. 1990, Vol 35, Num 4, pp 484-489, issn 0148-7299, 6 p.Article

Campomelia, polycystic dysplasia, and cervical lymphocele in two sibsURIOSTE, M; ARROYO, A; MARTINEZ-FRIAS, M.-L et al.American journal of medical genetics. 1991, Vol 41, Num 4, pp 475-477, issn 0148-7299Conference Paper

Segmentation anomalies of the vertebras and ribs : a developmental field defect : epidemiologic evidenceMARTINEZ-FRIAS, M. L; URIOSTE, M.American journal of medical genetics. 1994, Vol 49, Num 1, pp 36-44, issn 0148-7299Article

New case of limb body-wall complex associated with sirenomelia sequenceMARTINEZ-FRIAS, M. L; CUCALON, F; URIOSTE, M et al.American journal of medical genetics. 1992, Vol 44, Num 5, pp 583-585, issn 0148-7299Article

Characterization of the A673 cell line (Ewing tumor) by molecular cytogenetic techniquesMARTINEZ-RAMIREZ, A; RODRIGUEZ-PERALES, S; MELENDEZ, B et al.Cancer genetics and cytogenetics. 2003, Vol 141, Num 2, pp 138-142, issn 0165-4608, 5 p.Article

Proximal partial 5p trisomy resulting from a maternal (19;5) insertionLORDA-SANCHEZ, I; URIOSTE, M; VILLA, A et al.American journal of medical genetics. 1997, Vol 68, Num 4, pp 476-480, issn 0148-7299Article

Epidemiological analysis of multi-site closure failure of neural tube in humansMARTINEZ-FRIAS, M.-L; URIOSTE, M; BERMEJO, E et al.American journal of medical genetics. 1996, Vol 66, Num 1, pp 64-68, issn 0148-7299Article

De novo interstitial deletion q16.2q21 on chromosome 6VILLA, A; URIOSTE, M; BOFARULL, J. M et al.American journal of medical genetics. 1995, Vol 55, Num 3, pp 379-383, issn 0148-7299Article

Severe spondylocostal dysostosis associated with other congenital anomalies : a clinical/epidemiologic analysis and description of ten cases from the Spanish registryMARTINEZ-FRIAS, M.-L; BERMEJO, E; URIOSTE, M et al.American journal of medical genetics. 1994, Vol 51, Num 3, pp 203-212, issn 0148-7299Article

DK-phocomelia syndrome in a child with a long follow-upURIOSTE, M; PAISAN, L; MARTINEZ-FRIAS, M. L et al.American journal of medical genetics. 1994, Vol 52, Num 3, pp 269-271, issn 0148-7299Conference Paper

Clinical and genetic characterization of classical forms of familial adenomatous polyposis: a Spanish population studyRIVERA, B; GONZALEZ, S; SANCHEZ-TOME, E et al.Annals of oncology. 2011, Vol 22, Num 4, pp 903-909, issn 0923-7534, 7 p.Article

MLH1 germline epimutations in selected patients with early-onset non-polyposis colorectal cancerVALLE, L; CARBONELL, P; FERNANDEZ, V et al.Clinical genetics. 2007, Vol 71, Num 3, pp 232-237, issn 0009-9163, 6 p.Article

Analysis of the INK4a/ARF locus in non-Hodgkin's lymphomas using two new internal microsatellite markersHERRANZ, M; URIOSTE, M; SANTOS, J et al.Leukemia. 1999, Vol 13, Num 5, pp 808-810, issn 0887-6924Article

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