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

91 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Penetrance of mutations in the familial Wilms tumor gene FWT1.
Rahman N, Arbour L, Houlston R, Bonaïti-Pellié C, Abidi F, Tranchemontagne J, Ford D, Narod S, Pritchard-Jones K, Foulkes WD, Schwartz C, Stratton MR. Rahman N, et al. Among authors: abidi f. J Natl Cancer Inst. 2000 Apr 19;92(8):650-2. doi: 10.1093/jnci/92.8.650. J Natl Cancer Inst. 2000. PMID: 10772684 No abstract available.
Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1.
Rahman N, Abidi F, Ford D, Arbour L, Rapley E, Tonin P, Barton D, Batcup G, Berry J, Cotter F, Davison V, Gerrard M, Gray E, Grundy R, Hanafy M, King D, Lewis I, Ridolfi Luethy A, Madlensky L, Mann J, O'Meara A, Oakhill T, Skolnick M, Strong L, Stratton MR, et al. Rahman N, et al. Among authors: abidi f. Hum Genet. 1998 Nov;103(5):547-56. doi: 10.1007/pl00008708. Hum Genet. 1998. PMID: 9860296
Holmes-Gang syndrome is allelic with XLMR-hypotonic face syndrome.
Stevenson RE, Abidi F, Schwartz CE, Lubs HA, Holmes LB. Stevenson RE, et al. Among authors: abidi f. Am J Med Genet. 2000 Oct 23;94(5):383-5. doi: 10.1002/1096-8628(20001023)94:5<383::aid-ajmg7>3.0.co;2-7. Am J Med Genet. 2000. PMID: 11050622 No abstract available.
Cognitive function in Coffin-Lowry syndrome.
Simensen RJ, Abidi F, Collins JS, Schwartz CE, Stevenson RE. Simensen RJ, et al. Among authors: abidi f. Clin Genet. 2002 Apr;61(4):299-304. doi: 10.1034/j.1399-0004.2002.610410.x. Clin Genet. 2002. PMID: 12030896
Carpenter-Waziri syndrome results from a mutation in XNP.
Abidi F, Schwartz CE, Carpenter NJ, Villard L, Fontés M, Curtis M. Abidi F, et al. Am J Med Genet. 1999 Jul 30;85(3):249-51. doi: 10.1002/(sici)1096-8628(19990730)85:3<249::aid-ajmg12>3.0.co;2-u. Am J Med Genet. 1999. PMID: 10398237 No abstract available.
91 results