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Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay
by
Fryssira, H
,
Tsoutsou, E
,
Psoni, S
,
Amenta, S
,
Liehr, T
,
Anastasakis, E
,
Skentou, Ch
,
Ntouflia, A
,
Papoulidis, I
,
Manolakos, E
,
Chaliasos, N
Published in
Molecular cytogenetics
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Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay
by
Fryssira, H
,
Tsoutsou, E
,
Psoni, S
,
Amenta, S
,
Liehr, T
,
Anastasakis, E
,
Skentou, Ch
,
Ntouflia, A
,
Papoulidis, I
,
Manolakos, E
,
Chaliasos, N
Published in
Molecular cytogenetics
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Molecular Cytogenetics
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Array-Cgh
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Care And Treatment
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Case Report
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Case Studies
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Cytogenetics
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Foxg1 Syndrome
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Genetic Disorders
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Genetics & Heredity
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Life Sciences & Biomedicine
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Nova1
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Postnatal Microcephaly
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Rett Syndrome
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