Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 130

1.
2.

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.

Hamosh A, Scott AF, Amberger J, Bocchini C, Valle D, McKusick VA.

Nucleic Acids Res. 2002 Jan 1;30(1):52-5.

3.

Genomics of human dysmorphogenesis.

Wilson GN.

Am J Med Genet. 1992 Jan 15;42(2):187-96.

PMID:
1733168
4.

The morbid anatomy of the human genome: a review of gene mapping in clinical medicine (3).

McKusick VA.

Medicine (Baltimore). 1987 Jul;66(4):237-96. Review. No abstract available.

PMID:
3298930
5.

A gene map of congenital malformations.

Wilkie AO, Amberger JS, McKusick VA.

J Med Genet. 1994 Jul;31(7):507-17. Review.

6.
7.

The morbid anatomy of the human genome: a review of gene mapping in clinical medicine. 4.

McKusick VA.

Medicine (Baltimore). 1988 Jan;67(1):1-19. Review. No abstract available.

PMID:
2892112
8.

Synteny-defined candidate genes for congenital and idiopathic scoliosis.

Giampietro PF, Raggio CL, Blank RD.

Am J Med Genet. 1999 Mar 19;83(3):164-77.

PMID:
10096591
9.

The human obesity gene map: the 2000 update.

Pérusse L, Chagnon YC, Weisnagel SJ, Rankinen T, Snyder E, Sands J, Bouchard C.

Obes Res. 2001 Feb;9(2):135-69. Review.

10.

The status of online Mendelian inheritance in man (OMIM) medio 1994.

Pearson P, Francomano C, Foster P, Bocchini C, Li P, McKusick V.

Nucleic Acids Res. 1994 Sep;22(17):3470-3.

11.

The human obesity gene map: the 2004 update.

Pérusse L, Rankinen T, Zuberi A, Chagnon YC, Weisnagel SJ, Argyropoulos G, Walts B, Snyder EE, Bouchard C.

Obes Res. 2005 Mar;13(3):381-490.

12.

The morbid anatomy of the human genome: chromosomal location of mutations causing disease (update 1 December 1993).

McKusick VA, Amberger JS.

J Med Genet. 1994 Apr;31(4):265-79. Review. No abstract available.

13.

Online Mendelian Inheritance in Man (OMIM).

Hamosh A, Scott AF, Amberger J, Valle D, McKusick VA.

Hum Mutat. 2000;15(1):57-61.

PMID:
10612823
14.

Chromosome rearrangements and human gene mapping.

Gilgenkrantz S, Philippe C, Chery M.

Biomed Pharmacother. 1994;48(5-6):225-30.

PMID:
7999983
15.

Clinical genetics: an overview.

Nehring WM, Faux SA.

J Cardiovasc Nurs. 1999 Jul;13(4):19-33. Review.

PMID:
10386269
16.

General mutation databases: analysis and review.

George RA, Smith TD, Callaghan S, Hardman L, Pierides C, Horaitis O, Wouters MA, Cotton RG.

J Med Genet. 2008 Feb;45(2):65-70. Epub 2007 Sep 24. Review.

17.

The analysis of inconsistencies between cytogenetic annotations and sequence mapping by defining the imprecision zones of cytogenetic banding.

Yen KH, Ho CL, Lee C.

Bioinformatics. 2009 Apr 1;25(7):845-52. doi: 10.1093/bioinformatics/btn649. Epub 2008 Dec 20.

PMID:
19098301
18.

Genomic alterations and instabilities in renal cell carcinomas and their relationship to tumor pathology.

Thrash-Bingham CA, Salazar H, Freed JJ, Greenberg RE, Tartof KD.

Cancer Res. 1995 Dec 15;55(24):6189-95.

19.

The human obesity gene map: the 1998 update.

Pérusse L, Chagnon YC, Weisnagel J, Bouchard C.

Obes Res. 1999 Jan;7(1):111-29. Review.

20.

GFINDer: genetic disease and phenotype location statistical analysis and mining of dynamically annotated gene lists.

Masseroli M, Galati O, Pinciroli F.

Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W717-23.

Supplemental Content

Support Center