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Items: 2

1.

Genome-wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation.

Borck G, Rio M, Sanlaville D, Redon R, Molinari F, Bacq D, Raoul O, Cormier-Daire V, Lyonnet S, Amiel J, Le Merrer M, de Blois MC, Prieur M, Vekemans M, Carter NP, Munnich A, Colleaux L.

Clin Genet. 2004 Aug;66(2):122-7.

PMID:
15253762
2.

Cryptic duplication of 21q in an individual with a clinical diagnosis of Down syndrome.

Forster-Gibson CJ, Davies J, MacKenzie JJ, Harrison K.

Clin Genet. 2001 Jun;59(6):438-43.

PMID:
11453976

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