Faustina Lalatta

Cryptic deletions are a common finding in “balanced” reciprocal and complex chromosome rearrangements: a study of 59 patients

Manuela De Gregori, Roberto Ciccone, Pamela Magini et al. · Journal of Medical Genetics · 2007 · 357 citations · Full text

Life Sciences, Genetics, Cytogenetics +16

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith–Wiedemann syndrome

Jet Bliek, Gaetano Verde, Jonathan L A Callaway et al. · European Journal of Human Genetics · 2008 · 232 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Fertility in a 47,XXY patient: assessment of biological paternity by deoxyribonucleic acid fingerprinting

G. L. Terzoli, Faustina Lalatta, A. Lobbiani et al. · Fertility and Sterility · 1992 · 193 citations

Medicine, Genetics, Molecular Genetics +14

<i>De novo</i> balanced chromosome rearrangements in prenatal diagnosis

Daniela Giardino, Cecilia Corti, Lucia Ballarati et al. · Prenatal Diagnosis · 2009 · 142 citations · Full text

Life Sciences, Genetics, Human Genetics +16

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports

Laura Bernardini, Stefania Gimelli, Cristina Gervasini et al. · Orphanet Journal of Rare Diseases · 2009 · 142 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17