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Article

Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.

Cytogenetic and genome research - 1 Jan 2006

Krepischi-Santos A C V, Vianna-Morgante A M, Jehee F S, Passos-Bueno M R, Knijnenburg J, Szuhai K, Sloos W, Mazzeu J F, Kok F, Cheroki C, Otto P A, Mingroni-Netto R C, Varela M, Koiffmann C, Kim C A, Bertola D R, Pearson P L, Rosenberg C

Abstract excerpt

We report array-CGH screening of 95 syndromic patients with normal G-banded karyotypes and at least one of the following features: mental retardation, heart defects, deafness, obesity, craniofacial dysmorphisms or urogenital tract malformations. Chromosome imbalances not previously detected in no...

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Identifiers

PMID: 17124408
DOI: 10.1159/000095922

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17124408-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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