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

• Asıl Yazarlar: Rosaria Nardello (Yazar), Vincenzo Antona (Yazar), Giuseppe Donato Mangano (Yazar), Vincenzo Salpietro (Yazar), Salvatore Mangano (Yazar), Antonina Fontana (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: BMC, 2021-04-01T00:00:00Z.
• Konular: article
• Online Erişim: 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...