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Deletion of chr7p22 and chr15q11: Two Familial Cases of Immune Deficiency: Extending the Phenotype Toward Dysimmunity. https://t.co/nu0k1cJHhA https://t.co/ccQEzt1baN
Deletion of chr7p22 and chr15q11: Two Familial Cases of Immune Deficiency: Extending the Phenotype Toward Dysimmunity. https://t.co/nu0k1cJHhA https://t.co/ccQEzt1baN
New Research: Deletion of chr7p22 and chr15q11: Two Familial Cases of Immune Deficiency: Extending the Phenotype Toward Dysimmunity: Background: We report here two new familial cases of associated del15q11 and del7p22, with the latter… https://t.co/mxmnbz5