Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 27


Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases.

MaciÄ…g A, Villa F, Ferrario A, Spinelli CC, Carrizzo A, Malovini A, Torella A, Montenero C, Parisi A, Condorelli G, Vecchione C, Nigro V, Montenero AS, Puca AA.

BMC Genet. 2015 Feb 11;16:15. doi: 10.1186/s12863-015-0177-0.


Molecular characteristics of endometrial cancer coexisting with peritoneal malignant mesothelioma in Li-Fraumeni-like syndrome.

Chao A, Lai CH, Lee YS, Ueng SH, Lin CY, Wang TH.

BMC Cancer. 2015 Jan 15;15:8. doi: 10.1186/s12885-015-1010-x.


Genetic dissection of two Pakistani families with consanguineous localized autosomal recessive hypotrichosis (LAH).

Abbas S, Naveed AK, Khan S, Yousaf MJ, Azeem Z, Razak S, Qaiser F.

Iran J Basic Med Sci. 2014 Jul;17(7):470-5.


Helium: visualization of large scale plant pedigrees.

Shaw PD, Graham M, Kennedy J, Milne I, Marshall DF.

BMC Bioinformatics. 2014 Aug 1;15:259. doi: 10.1186/1471-2105-15-259.


Routes for breaching and protecting genetic privacy.

Erlich Y, Narayanan A.

Nat Rev Genet. 2014 Jun;15(6):409-21. doi: 10.1038/nrg3723. Epub 2014 May 8. Review. Erratum in: Nat Rev Genet. 2014 Aug;15(8):570.


Family history in primary care pediatrics.

Tarini BA, McInerney JD.

Pediatrics. 2013 Dec;132(Suppl 3):S203-10. doi: 10.1542/peds.2013-1032D.


Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance.

Bonnen PE, Yarham JW, Besse A, Wu P, Faqeih EA, Al-Asmari AM, Saleh MA, Eyaid W, Hadeel A, He L, Smith F, Yau S, Simcox EM, Miwa S, Donti T, Abu-Amero KK, Wong LJ, Craigen WJ, Graham BH, Scott KL, McFarland R, Taylor RW.

Am J Hum Genet. 2013 Sep 5;93(3):471-81. doi: 10.1016/j.ajhg.2013.07.017. Epub 2013 Aug 29. Erratum in: Am J Hum Genet. 2013 Oct 3;93(4):773.


The family medical history as a tool in preconception consultation.

Bennett RL.

J Community Genet. 2012 Jul;3(3):175-83. doi: 10.1007/s12687-012-0107-z. Epub 2012 Jul 19.


The use of genealogy databases for risk assessment in genetic health service: a systematic review.

Stefansdottir V, Johannsson OT, Skirton H, Tryggvadottir L, Tulinius H, Jonsson JJ.

J Community Genet. 2013 Jan;4(1):1-7. doi: 10.1007/s12687-012-0103-3. Epub 2012 Jul 18.


VIPER: a visualisation tool for exploring inheritance inconsistencies in genotyped pedigrees.

Paterson T, Graham M, Kennedy J, Law A.

BMC Bioinformatics. 2012;13 Suppl 8:S5. doi: 10.1186/1471-2105-13-S8-S5. Epub 2012 May 18.


Using a family history intervention to improve cancer risk perception in a black community.

Murthy VS, Garza MA, Almario DA, Vogel KJ, Grubs RE, Gettig EA, Wilson JW, Thomas SB.

J Genet Couns. 2011 Dec;20(6):639-49. doi: 10.1007/s10897-011-9389-2. Epub 2011 Jul 20.


Population-based proband-oriented pedigree information system: application to hypertension with population-based screening data (KCIS No. 25).

Chiu SY, Chen LS, Yen AM, Chen HH.

J Am Med Inform Assoc. 2012 Jan-Feb;19(1):102-10. doi: 10.1136/amiajnl-2010-000059. Epub 2011 Jul 4.


Identification of missense mutation (I12T) in the BSND gene and bioinformatics analysis.

Iqbal H, Sarfaraz T, Anjum F, Anwar Z, Mir A.

J Biomed Biotechnol. 2011;2011:304612. doi: 10.1155/2011/304612. Epub 2011 Apr 4.


Validation of My Family Health Portrait for six common heritable conditions.

Facio FM, Feero WG, Linn A, Oden N, Manickam K, Biesecker LG.

Genet Med. 2010 Jun;12(6):370-5. doi: 10.1097/GIM.0b013e3181e15bd5.


A homozygous p.Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa.

Azam M, Khan MI, Gal A, Hussain A, Shah ST, Khan MS, Sadeque A, Bokhari H, Collin RW, Orth U, van Genderen MM, den Hollander AI, Cremers FP, Qamar R.

Mol Vis. 2009 Dec 3;15:2526-34.


The family history: reemergence of an established tool.

Hinton RB Jr.

Crit Care Nurs Clin North Am. 2008 Jun;20(2):149-58, v. doi: 10.1016/j.ccell.2008.01.004. Review.


Sex symbols ancient and modern: their origins and iconography on the pedigree.

Schott GD.

BMJ. 2005 Dec 24;331(7531):1509-10. No abstract available.

Supplemental Content

Support Center