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letter . 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 Vincent
, S Julia
, G Bourrouillou
, P Calvas
, E Bieth
P De Mas
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N Chassaing
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Y Chaix
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M Vincent
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S Julia
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G Bourrouillou
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P Calvas
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E Bieth
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PMCID: PMC1735090 PMID: 11950869