Agenesis of the corpus callosum with Probst bundles owing to haploinsufficiency for a gene in an 8 cM region of 6q25.

Author:

Pirola B,Bortotto L,Giglio S,Piovan E,Janes A,Guerrini R,Zuffardi O

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference16 articles.

1. Absence makes the search grow longer;Dobyns, W.B.;Am J Hum Genet,1996

2. Multiple congenital anomalies, brain hypomyelinization and ocular albinism in a female with dup(X)(pter-q24::q21.32-qter) and random X inactivation;Carrozzo, R.; Arrigo, G.; Rossi, E.;AmJMed Genet,1997

3. The same molecular mechanism at the maternal meiosis I produces monoand dicentric 8p duplications;Floridia, G.; Piantanida, M.; Minelli, A.;Am J Hum Genet,1996

4. Epidemiology of central nervous system malformations;Myrianthopoulos, N.C.,1977

5. Frequency of agenesis of the corpus callosum in the developmentally disabled population as determined by computerized tomography;Jeret, J.S.; Serur, D.; Wisniewski, K.; Fisch, C.;Pediatr Neurosci,1985

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