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Exploring the clinical and epidemiological complexity of GJB2-linked deafness.
Am J Med Genet. 2002 Sep 15;112(1):38-45. doi: 10.1002/ajmg.10621.
Am J Med Genet. 2002.
PMID: 12239718
Prenatal UPD testing survey in Robertsonian translocations.
Gualandi F, Sensi A, Trabanelli C, Falciano F, Bonfatti A, Calzolari E.
Gualandi F, et al. Among authors: falciano f.
Prenat Diagn. 2000 Jun;20(6):465-8.
Prenat Diagn. 2000.
PMID: 10861710
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Mole maker phenotype: possible narrowing of the candidate region.
Sensi A, Gualandi F, Pittalis MC, Calabrese O, Falciano F, Maestri I, Bovicelli L, Calzolari E.
Sensi A, et al. Among authors: falciano f.
Eur J Hum Genet. 2000 Aug;8(8):641-4. doi: 10.1038/sj.ejhg.5200501.
Eur J Hum Genet. 2000.
PMID: 10951527
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