Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 173

1.

NBCCS secondary to an interstitial chromosome 9q deletion.

Haniffa MA, Leech SN, Lynch SA, Simpson NB.

Clin Exp Dermatol. 2004 Sep;29(5):542-4.

PMID:
15347344
2.

Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndrome.

Midro AT, Panasiuk B, Tümer Z, Stankiewicz P, Silahtaroglu A, Lupski JR, Zemanova Z, Stasiewicz-Jarocka B, Hubert E, Tarasów E, Famulski W, Zadrozna-Tołwińska B, Wasilewska E, Kirchhoff M, Kalscheuer V, Michalova K, Tommerup N.

Am J Med Genet A. 2004 Jan 15;124A(2):179-91. Review.

PMID:
14699618
3.

Further delineation of 9q22 deletion syndrome associated with basal cell nevus (Gorlin) syndrome: report of two cases and review of the literature.

Yamamoto K, Yoshihashi H, Furuya N, Adachi M, Ito S, Tanaka Y, Masuno M, Chiyo H, Kurosawa K.

Congenit Anom (Kyoto). 2009 Mar;49(1):8-14. doi: 10.1111/j.1741-4520.2008.00212.x.

PMID:
19243411
4.

Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome.

Boonen SE, Stahl D, Kreiborg S, Rosenberg T, Kalscheuer V, Larsen LA, Tommerup N, Brøndum-Nielsen K, Tümer Z.

Am J Med Genet A. 2005 Jan 30;132A(3):324-8. Review.

PMID:
15690381
5.

Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas.

Schofield D, West DC, Anthony DC, Marshal R, Sklar J.

Am J Pathol. 1995 Feb;146(2):472-80.

6.

Molecular analysis of chromosome 9q deletions in two Gorlin syndrome patients.

Shimkets R, Gailani MR, Siu VM, Yang-Feng T, Pressman CL, Levanat S, Goldstein A, Dean M, Bale AE.

Am J Hum Genet. 1996 Aug;59(2):417-22.

7.

Gorlin syndrome patient with large deletion in 9q22.32-q22.33 detected by quantitative multiplex fluorescent PCR.

Musani V, Cretnik M, Situm M, Basta-Juzbasic A, Levanat S.

Dermatology. 2009;219(2):111-8. doi: 10.1159/000219247. Epub 2009 May 14. Review.

PMID:
19439922
8.

Investigation of chromosome 9q22.3-q31 DNA marker loss in odontogenic keratocysts.

Lench NJ, High AS, Markham AF, Hume WJ, Robinson PA.

Eur J Cancer B Oral Oncol. 1996 May;32B(3):202-6.

PMID:
8762878
9.

Nevoid basal cell carcinoma syndrome.

Bale AE, Gailani MR, Leffell DJ.

J Invest Dermatol. 1994 Nov;103(5 Suppl):126S-130S. Review.

PMID:
7963674
10.

Delineation of two distinct deleted regions on chromosome 9 in human non-melanoma skin cancers.

Quinn AG, Sikkink S, Rees JL.

Genes Chromosomes Cancer. 1994 Dec;11(4):222-5.

PMID:
7533525
11.

Hypoplastic thumb in Gorlin's syndrome.

Kansal A, Brueton L, Lahiri A, Lester R.

J Plast Reconstr Aesthet Surg. 2007;60(4):440-2. Epub 2006 Sep 7.

PMID:
17349603
12.

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome.

Hahn H, Wicking C, Zaphiropoulous PG, Gailani MR, Shanley S, Chidambaram A, Vorechovsky I, Holmberg E, Unden AB, Gillies S, Negus K, Smyth I, Pressman C, Leffell DJ, Gerrard B, Goldstein AM, Dean M, Toftgard R, Chenevix-Trench G, Wainwright B, Bale AE.

Cell. 1996 Jun 14;85(6):841-51.

13.

Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosity.

Chenevix-Trench G, Wicking C, Berkman J, Sharpe H, Hockey A, Haan E, Oley C, Ravine D, Turner A, Goldgar D, et al.

Am J Hum Genet. 1993 Sep;53(3):760-7.

14.

Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel-type zinc finger sequence on chromosome segment 9q22.3.

Chidambaram A, Gailani M, Gerrard B, Stewart C, Goldstein A, Chumakov I, Bale AE, Dean M.

Genes Chromosomes Cancer. 1997 Mar;18(3):212-8.

PMID:
9071574
16.

Developmental genes and cancer: role of patched in basal cell carcinoma of the skin.

Gailani MR, Bale AE.

J Natl Cancer Inst. 1997 Aug 6;89(15):1103-9. Review.

PMID:
9262247
17.

Multiple tumor types including leiomyoma and Wilms tumor in a patient with Gorlin syndrome due to 9q22.3 microdeletion encompassing the PTCH1 and FANC-C loci.

Garavelli L, Piemontese MR, Cavazza A, Rosato S, Wischmeijer A, Gelmini C, Albertini E, Albertini G, Forzano F, Franchi F, Carella M, Zelante L, Superti-Furga A.

Am J Med Genet A. 2013 Nov;161A(11):2894-901. doi: 10.1002/ajmg.a.36259. Epub 2013 Oct 7.

PMID:
24124115
18.

Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome.

Olivieri C, Maraschio P, Caselli D, Martini C, Beluffi G, Maserati E, Danesino C.

Eur J Pediatr. 2003 Feb;162(2):100-3. Epub 2002 Dec 10.

PMID:
12548386
19.

[A nevoid basal cell carcinoma syndrome with chromosomal aberration].

Sasaki K, Yoshimoto T, Nakao T, Minagawa K, Takahashi Y, Watanabe Y, Tanabe C.

No To Hattatsu. 2000 Jan;32(1):49-55. Review. Japanese.

PMID:
10655752
20.

Parental origin of chromosome 9q22.3-q31 lost in basal cell carcinomas from basal cell nevus syndrome patients.

Bonifas JM, Bare JW, Kerschmann RL, Master SP, Epstein EH Jr.

Hum Mol Genet. 1994 Mar;3(3):447-8.

PMID:
8012356

Supplemental Content

Support Center