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Journal De Genetique Humaine|October 1, 1977
Trisomy for the short arm of chromosome No. 10V B Penchaszadeh, R CocoJournal De Genetique Humaine|September 1, 1978
Inherited parital duplication deficiency of chromosome 15 (p12;q22)R Coco, V B PenchaszadehAmerican Journal of Medical Genetics|June 1, 1982
Cytogenetic findings in 200 children with mental retardation and multiple congenital anomalies of unknown causeR Coco, V B PenchaszadehActa Endocrinologica|December 1, 1975
Asymmetrical gonadal differentiation and gonadoblastoma. Clinical, cytogenetic and histological findings. Case reportR Coco, H Chemes, C BergadaAmerican Journal of Medical Genetics|June 13, 1997
Patient with an Xp21 contiguous gene deletion syndrome in association with agenesis of the corpus callosumS E Baranzini, G del Rey, N Nigro, et al.Ginecologia Y Obstetricia De Mexico|August 1, 1989
[C-reactive protein as early marker of chorioamnionitis in premature rupture of membranes]V Ibarra Chavarría, P Sanhueza Smith, M Mota González, et al.Archives of Medical Research|September 18, 1997
Assessment of the functional capacity for intracellular death and phagocytosis of polymorphonuclear cells in healthy neonatesG Del Rey-Pineda, M V Gómez-González, F Solórzano-Santos, et al.Journal De Genetique Humaine|March 1, 1978
Ovarian differentiation in Turner's syndromeC F Rivelis, R Coco, C BergadaAnnales De Genetique|June 1, 1975
A case of ring 18 chromosome in a sibship with multiple spontaneous abortionsR Coco, C Z Barreiro, V B PenchaszadehAndrology|January 20, 2015
Is a CIS phenotype apparent in children with Disorders of Sex Development? Milder testicular dysgenesis is associated with a higher risk of malignancyH E Chemes, M Venara, G Del Rey, et al.Pageof 5