Mutations in mammalian tolloid-like 1 gene detected in adult patients with ASD

Author:

Stańczak Paweł,Witecka Joanna,Szydło Anna,Gutmajster Ewa,Lisik Małgorzata,Auguściak-Duma Aleksandra,Tarnowski Maciej,Czekaj Tomasz,Czekaj Hanna,Sieroń Aleksander L

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference43 articles.

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2. Boughman JA, Berg KA, Astemborski JA et al: Familial risks of congenital heart defect assessed in a population based epidemiologic study. Am J Med Genet 1987; 26: 839–849.

3. Van Mierop LHS : Embryology of the atrioventricular canal region and pathogenesis of endocardial cushion defects; in Feldt RH, McGoon DC, Ongley PA, Rastelli GC, Titus JL, Van Mierop LHS (eds): Atrioventricular Canal Defects. Philadelphia, PA: WB Saunders, 1976, pp 1–12.

4. Hoffman JI : Congenital heart disease: incidence and inheritance. Pediatr Clin North Am 1990; 37: 25–43.

5. Fyler DC : Atrial septal defect secundum; in Fyler DC (ed): Nadas Pediatric Cardiology. Boston, MA: Mosby Year Book Inc., 1992, pp 513–524.

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