A 12Mb deletion at 7q33–q35 associated with autism spectrum disorders and primary amenorrhea

Author:

Rossi Elena,Verri Anna Pia,Patricelli Maria Grazia,Destefani Valeria,Ricca Ivana,Vetro Annalisa,Ciccone Roberto,Giorda Roberto,Toniolo Daniela,Maraschio Paola,Zuffardi Orsetta

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference25 articles.

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2. Autism genetic research exchange consortium. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families;Alarcón;Am. J. Hum. Genet.,2002

3. The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects;Aman;Am. J. Ment. Defic.,1985

4. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism;Arking;Am. J. Hum. Genet.,2008

5. TPL Test Primo Linguaggio;Axia,1995

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