Embryonic expression of the human MID 1 gene and its mutations in Opitz syndrome

Authors :: Meroni, G.
Lyonnet, S.
Vekemans, M.
Attie. Bitach, T.
Pinson, L.
Auge, J.
Audollent, S.
Mattei, G.
Etchevers, H.
Gigarel, N.
Razavi, F.
Lacombe, D.
Odent, S.
M Le Merrer
Amiel, J.
Munnich, A.
Source :: Journal of Medical Genetics. May, 2004, Vol. 41 Issue 5, p381, 6 p.
Publication Year :: 2004
Abstract: Opitz syndrome is a midline congenital malformation characterized by hypertelorism, hypospadias and oesophagolaryngotracheal defects, which leads to swallowing difficulties and hoarse voice. The role of MID 1 during embryonic development is investigated through expression studies.

Subjects :: Genes -- Analysis
Throat diseases -- Genetic aspects
Throat diseases -- Research
Genetic research
Health

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