Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 104

1.

Microdeletion of 22q11.1 is associated with two cases of familial nonsyndromic basal cell carcinoma.

Naderi A.

Cancer Genet Cytogenet. 2010 Oct 15;202(2):133-5. doi: 10.1016/j.cancergencyto.2010.07.123.

PMID:
20875876
2.

Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome.

de Ravel TJ, Ameye L, Ballon K, Borghgraef M, Vermeesch JR, Devriendt K.

Eur J Med Genet. 2009 Mar-Jun;52(2-3):145-7. doi: 10.1016/j.ejmg.2009.02.002. Epub 2009 Feb 21.

PMID:
19233320
3.

Familial recurrence of nonsyndromic congenital heart defects in first degree relatives of patients with deletion 22q11.2.

Digilio MC, Marino B, Capolino R, Angioni A, Sarkozy A, Roberti MC, Conti E, de Zorzi A, Dallapiccola B.

Am J Med Genet A. 2005 Apr 15;134A(2):158-64.

PMID:
15669097
4.

Higher frequency of uncommon 1.5-2 Mb deletions found in familial cases of 22q11.2 deletion syndrome.

Fernández L, Lapunzina P, Pajares IL, Criado GR, García-Guereta L, Pérez J, Quero J, Delicado A.

Am J Med Genet A. 2005 Jul 1;136(1):71-5.

PMID:
15889418
5.

PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and inherited human basal cell carcinomas.

Santos DC, Zaphiropoulos PG, Neto CF, Pimentel ER, Sanches JA Jr, Ruiz IR.

Int J Dermatol. 2011 Jul;50(7):838-43. doi: 10.1111/j.1365-4632.2010.04866.x.

PMID:
21699520
6.

Analysis of p53 gene mutations and loss of heterozygosity for loci on chromosome 9q in basal cell carcinoma.

Konishi K, Yamanishi K, Ishizaki K, Yamada K, Kishimoto S, Yasuno H.

Cancer Lett. 1994 Apr 29;79(1):67-72.

PMID:
8187055
7.

BAC array CGH in patients with Velocardiofacial syndrome-like features reveals genomic aberrations on chromosome region 1q21.1.

Brunet A, Armengol L, Heine D, Rosell J, García-Aragonés M, Gabau E, Estivill X, Guitart M.

BMC Med Genet. 2009 Dec 23;10:144. doi: 10.1186/1471-2350-10-144.

8.

Relationship between sunlight exposure and a key genetic alteration in basal cell carcinoma.

Gailani MR, Leffell DJ, Ziegler A, Gross EG, Brash DE, Bale AE.

J Natl Cancer Inst. 1996 Mar 20;88(6):349-54.

9.

Genetic background of congenital conotruncal heart defects--a study of 45 families.

Kwiatkowska J, Wierzba J, Aleszewicz-Baranowska J, Ereciński J.

Kardiol Pol. 2007 Jan;65(1):32-7; discussion 38-9. English, Polish.

10.

Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer.

Holmberg E, Rozell BL, Toftgård R.

Br J Cancer. 1996 Jul;74(2):246-50.

11.

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.

12.

Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.

Beauchesne LM, Warnes CA, Connolly HM, Ammash NM, Grogan M, Jalal SM, Michels VV.

J Am Coll Cardiol. 2005 Feb 15;45(4):595-8.

13.

Clinical features of microdeletion 9q22.3 (pat).

Shimojima K, Adachi M, Tanaka M, Tanaka Y, Kurosawa K, Yamamoto T.

Clin Genet. 2009 Apr;75(4):384-93. doi: 10.1111/j.1399-0004.2008.01141.x.

PMID:
19320658
14.

Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas.

Reifenberger J, Wolter M, Knobbe CB, Köhler B, Schönicke A, Scharwächter C, Kumar K, Blaschke B, Ruzicka T, Reifenberger G.

Br J Dermatol. 2005 Jan;152(1):43-51.

PMID:
15656799
15.

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
16.

Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney.

Wieser R, Fritz B, Ullmann R, Müller I, Galhuber M, Storlazzi CT, Ramaswamy A, Christiansen H, Shimizu N, Rehder H.

Hum Mutat. 2005 Aug;26(2):78-83.

PMID:
15957176
17.

Detection of loss of heterozygosity on chromosome 9q22.3 in microdissected sporadic basal cell carcinoma.

Shen T, Park WS, Böni R, Saini N, Pham T, Lash AE, Vortmeyer AO, Zhuang Z.

Hum Pathol. 1999 Mar;30(3):284-7.

PMID:
10088546
18.
19.

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
20.

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
Items per page

Supplemental Content

Write to the Help Desk