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Case Reports
. 2002 Apr;39(4):e17.
doi: 10.1136/jmg.39.4.e17.

Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome

P De Mas, N Chassaing, Y Chaix, M-C Vincent, S Julia, G Bourrouillou, P Calvas, E Bieth
Case Reports

Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome

P De Mas et al. J Med Genet. 2002 Apr.
No abstract available

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