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American Journal of Medical Genetics|December 18, 2001
FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardationA E Cockwell, I P Dávalos, H R Rivera, et al.
Clinical Dysmorphology|October 29, 2002
Guadalajara camptodactyly type III: a new probably autosomal dominant syndromeL E Figuera, M L Ramírez-Dueñas, I P Dávalos, et al.
Annales De Genetique|May 20, 2000
inv(9)(p24q13) in three sterile brothersI P Dávalos, F Rivas, A L Ramos, et al.
Gynecologic and Obstetric Investigation|June 1, 2000
Reproductive history in mothers of children with neural tube defectsF Rivas, I P Dávalos, N Olivares, et al.
Genetic Counseling (Geneva, Switzerland)|May 3, 2003
A variant example of familial Floating-Harbor syndrome?J M Peñaloza, D García-Cruz, I P Dávalos, et al.
Cytogenetic and Genome Research|November 11, 2010
Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidismA I Vásquez-Velásquez, H A García-Castillo, M G González-Mercado, et al.
Annales De Genetique|September 22, 2000
The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populationsI P Dávalos, N Olivares, M T Castillo, et al.
Genetic Counseling (Geneva, Switzerland)|November 3, 2005
Zimmermann-Laband syndrome: further clinical delineationI P Dávalos, D García-Cruz, M O García-Cruz, et al.
The British Journal of Dermatology|November 26, 2005
A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalpN O Dávalos, A García-Vargas, J Pforr, et al.
The Pharmacogenomics Journal|June 2, 2010
Polymorphisms C677T and A1298C in the MTHFR gene in Mexican patients with rheumatoid arthritis treated with methotrexate: implication with elevation of transaminasesJ P Mena, M Salazar-Páramo, L González-López, et al.
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