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No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.

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Title: No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.
Authors: Schlögel, Matthieu J1 (AUTHOR), Mendola, Antonella1 (AUTHOR), Fastré, Elodie1 (AUTHOR), Vasudevan, Pradeep2 (AUTHOR), Devriendt, Koen3 (AUTHOR), de Ravel, Thomy JL3 (AUTHOR), Van Esch, Hilde3 (AUTHOR), Casteels, Ingele4 (AUTHOR), Carrera, Ignacio Arroyo5 (AUTHOR), Cristofoli, Francesca3 (AUTHOR), Fieggen, Karen6 (AUTHOR), Jones, Katheryn7 (AUTHOR), Lipson, Mark7 (AUTHOR), Balikova, Irina8 (AUTHOR), Singer, Ami9 (AUTHOR), Soller, Maria10 (AUTHOR), Villanueva, María Mercedes11 (AUTHOR), Revencu, Nicole1,12 (AUTHOR), Boon, Laurence M1,13 (AUTHOR), Brouillard, Pascal1 (AUTHOR)
Source: Orphanet Journal of Rare Diseases. May2015, Vol. 10 Issue 1, p52-62. 11p. 1 Color Photograph, 1 Diagram, 1 Chart, 2 Graphs.
Database: Academic Search Ultimate
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  Data: No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.
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  Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. May2015, Vol. 10 Issue 1, p52-62. 11p. 1 Color Photograph, 1 Diagram, 1 Chart, 2 Graphs.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=108311197
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