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Abbreviation : OS
Long Form : Opitz syndrome
No. Year Title Co-occurring Abbreviation
2016 Mid1/Mid2 expression in craniofacial development and a literature review of X-linked opitz syndrome. ---
2013 X-linked microtubule-associated protein, Mid1, regulates axon development. MID1
2006 A structure-function study of MID1 mutations associated with a mild Opitz phenotype. FNIII
2005 Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations. LTE
2003 X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrum. ADOS, LTE, TRIM
2002 Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate development. ---
2001 Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit alpha 4. ---
2000 New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome. RBCC
1999 Duplications on human chromosome 22 reveal a novel Ret Finger Protein-like gene family with sense and endogenous antisense transcripts. ---
10  1999 Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle. ---
11  1999 The Opitz syndrome gene product, MID1, associates with microtubules. ---
12  1997 Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. MID1