A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes

• المؤلفون الرئيسيون: Rosaria Nardello (مؤلف), Vincenzo Antona (مؤلف), Giuseppe Donato Mangano (مؤلف), Vincenzo Salpietro (مؤلف), Salvatore Mangano (مؤلف), Antonina Fontana (مؤلف)
• التنسيق: كتاب
• منشور في: BMC, 2021-04-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Abstract Background Most studies relative to Y chromosome abnormalities are focused on the sexual developmental disorders. Recently, a few studies suggest that some genes located on Y chromosome may be related to different neurodevelopment disorders. Case presentation We report a child with sexual d...