Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

179 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material.
Mazzanti L, Cicognani A, Baldazzi L, Bergamaschi R, Scarano E, Strocchi S, Nicoletti A, Mencarelli F, Pittalis M, Forabosco A, Cacciari E. Mazzanti L, et al. Among authors: forabosco a. Am J Med Genet A. 2005 Jun 1;135(2):150-4. doi: 10.1002/ajmg.a.30569. Am J Med Genet A. 2005. PMID: 15880570
Noonan-like syndrome with loose anagen hair: a new syndrome?
Mazzanti L, Cacciari E, Cicognani A, Bergamaschi R, Scarano E, Forabosco A. Mazzanti L, et al. Among authors: forabosco a. Am J Med Genet A. 2003 Apr 30;118A(3):279-86. doi: 10.1002/ajmg.a.10923. Am J Med Genet A. 2003. PMID: 12673660
Heart disease in Turner's syndrome.
Mazzanti L, Prandstraller D, Tassinari D, Rubino I, Santucci S, Picchio FM, Forabosco A, Cacciari E. Mazzanti L, et al. Among authors: forabosco a. Helv Paediatr Acta. 1988 Aug;43(1-2):25-31. Helv Paediatr Acta. 1988. PMID: 3170246
Barber-Say Syndrome: report of a new case.
Mazzanti L, Bergamaschi R, Neri I, Perri A, Patrizi A, Cacciari E, Forabosco A. Mazzanti L, et al. Among authors: forabosco a. Am J Med Genet. 1998 Jun 30;78(2):188-91. Am J Med Genet. 1998. PMID: 9674915
[Comparative auxological findings in monosomy X].
Mazzanti L, Forabosco A, Cacciari E. Mazzanti L, et al. Among authors: forabosco a. Pathologica. 1983;75 Suppl:281-4. Pathologica. 1983. PMID: 6680431 Italian. No abstract available.
Distal 12p deletion in a stillborn infant.
Baroncini A, Avellini C, Neri C, Forabosco A. Baroncini A, et al. Among authors: forabosco a. Am J Med Genet. 1990 Jul;36(3):358-60. doi: 10.1002/ajmg.1320360324. Am J Med Genet. 1990. PMID: 2363438
Genes and translocations involved in POF.
Schlessinger D, Herrera L, Crisponi L, Mumm S, Percesepe A, Pellegrini M, Pilia G, Forabosco A. Schlessinger D, et al. Among authors: forabosco a. Am J Med Genet. 2002 Aug 15;111(3):328-33. doi: 10.1002/ajmg.10565. Am J Med Genet. 2002. PMID: 12210333 Review.
Pure segmental trisomy 1q42-qter in a boy with a severe phenotype.
Percesepe A, Lugli L, Pierluigi M, Cavani S, Malacarne M, Roversi MF, Ferrari F, Forabosco A. Percesepe A, et al. Among authors: forabosco a. Am J Med Genet A. 2007 Oct 1;143A(19):2339-42. doi: 10.1002/ajmg.a.31890. Am J Med Genet A. 2007. PMID: 17702013 No abstract available.
179 results