Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature

Auteur

Manolakos, E.; Sifakis, S.; Sotiriou, S.; Peitsidis, P.; Eleftheriades, M.; Mersinias, V.; Liehr, T.; Thomaidis, L.; Kitsos, G.; Papoulidis, I.; Petersen, M. B.; Orru, S.

Date

2012

DOI

10.1097/MCD.0b013e32834e9279

Sujet

PARTIAL TRISOMY

1Q

PHENOTYPE

REARRANGEMENTS

DIAGNOSIS

DELINEATION

CGH

Genetics & Heredity

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URI

http://hdl.handle.net/11615/30647

Collections

• Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]