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American Journal of Medical Genetics|September 15, 1993
Schwartz-Jampel syndrome: an atypical form?L E Figuera, F J Jimenez-Gil, M O García-Cruz, et al.Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Complete achromatopsia associated with skeletal anomalies: a new autosomal recessive syndromeJ E García-Ortiz, D García-Cruz, R Mendoza-Topete, 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.Annales De Genetique|January 1, 1989
De novo dir dup (1)(q3200----4200) in an adult. Further delineation of the pure 1q trisomy syndromeP Barros-Núñez, J Sánchez-Corona, A Rolón, 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.Ophthalmic Paediatrics and Genetics|March 1, 1990
A distinct dysmorphic syndrome with congenital glaucoma and probable autosomal recessive inheritanceD García-Cruz, R Mendoza, V Villar, et al.Clinical Genetics|November 1, 1995
Christian's spondylo-digital syndrome: second familial caseD García-Cruz, J M Cantú, F J García-Martínez, et al.Clinical Genetics|October 1, 1993
The Myhre syndrome: report of two casesD García-Cruz, L E Figuera, A Feria-Velazco, et al.Genetic Counseling (Geneva, Switzerland)|May 28, 2011
Wide clinical spectrum in Zimmermann-Laband syndromeI P Davalos, A J L Brambila-Tapia, N O Dávalos, et al.Pageof 1