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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 1
2001 2
2002 2
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2014 1
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2016 2
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Page 1
[Hand-foot-genital syndrome].
Mitsubuchi H, Endo F. Mitsubuchi H, et al. Nihon Rinsho. 2006 Jun 28;Suppl 2:647-8. Nihon Rinsho. 2006. PMID: 16817484 Review. Japanese. No abstract available.
Human HOX gene disorders.
Quinonez SC, Innis JW. Quinonez SC, et al. Mol Genet Metab. 2014 Jan;111(1):4-15. doi: 10.1016/j.ymgme.2013.10.012. Epub 2013 Oct 29. Mol Genet Metab. 2014. PMID: 24239177 Free article. Review.
Human HOX gene mutations.
Goodman FR, Scambler PJ. Goodman FR, et al. Clin Genet. 2001 Jan;59(1):1-11. doi: 10.1034/j.1399-0004.2001.590101.x. Clin Genet. 2001. PMID: 11206481 Review.
HOX genes play a fundamental role in the development of the vertebrate central nervous system, axial skeleton, limbs, gut, urogenital tract and external genitalia, but it is only in the last 4 years that mutations in two of the 39 human HOX genes have been shown to cause congenit …
HOX genes play a fundamental role in the development of the vertebrate central nervous system, axial skeleton, limbs, gut, urogenital tract …
[Hand-foot-genital syndrome].
Ieshima A. Ieshima A. Ryoikibetsu Shokogun Shirizu. 2001;(33):785-6. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462685 Review. Japanese. No abstract available.
Genetics of the female reproductive ducts.
Simpson JL. Simpson JL. Am J Med Genet. 1999 Dec 29;89(4):224-39. doi: 10.1002/(sici)1096-8628(19991229)89:4<224::aid-ajmg7>3.0.co;2-c. Am J Med Genet. 1999. PMID: 10727998 Review.
Single mutant genes (Mendelian) are responsible for the McKusick-Kaufman syndrome (MKS) and the hand-foot-genital syndrome. The molecular basis for the latter condition involves HOXA13, but the molecular basis of MKS and other disorders of the female r …
Single mutant genes (Mendelian) are responsible for the McKusick-Kaufman syndrome (MKS) and the hand-foot-genital sy …
HOX genes: seductive science, mysterious mechanisms.
Lappin TR, Grier DG, Thompson A, Halliday HL. Lappin TR, et al. Ulster Med J. 2006 Jan;75(1):23-31. Ulster Med J. 2006. PMID: 16457401 Free PMC article. Review.
The 39 human HOX genes are located in four clusters (A-D) on different chromosomes at 7p15, 17q21 [corrected] 12q13, and 2q31 respectively and are assumed to have arisen by duplication and divergence from a primordial homeobox gene. Disorders of limb formation, such as hand …
The 39 human HOX genes are located in four clusters (A-D) on different chromosomes at 7p15, 17q21 [corrected] 12q13, and 2q31 respectively a …
The pathophysiology of HOX genes and their role in cancer.
Grier DG, Thompson A, Kwasniewska A, McGonigle GJ, Halliday HL, Lappin TR. Grier DG, et al. J Pathol. 2005 Jan;205(2):154-71. doi: 10.1002/path.1710. J Pathol. 2005. PMID: 15643670 Review.
Mutations in HOXA13 and HOXD13 are associated with disorders of limb formation such as hand-foot-genital syndrome (HFGS), synpolydactyly (SPD), and brachydactyly. ...
Mutations in HOXA13 and HOXD13 are associated with disorders of limb formation such as hand-foot-genital syndrome …
Limb malformations and the human HOX genes.
Goodman FR. Goodman FR. Am J Med Genet. 2002 Oct 15;112(3):256-65. doi: 10.1002/ajmg.10776. Am J Med Genet. 2002. PMID: 12357469 Review.
The first two limb malformations shown to be caused by mutations in the human HOX genes were synpolydactyly and hand-foot-genital syndrome, which result from mutations in HOXD13 and HOXA13, respectively. ...
The first two limb malformations shown to be caused by mutations in the human HOX genes were synpolydactyly and hand-foot-g …
A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?
Utsch B, Becker K, Brock D, Lentze MJ, Bidlingmaier F, Ludwig M. Utsch B, et al. Hum Genet. 2002 May;110(5):488-94. doi: 10.1007/s00439-002-0712-8. Epub 2002 Apr 4. Hum Genet. 2002. PMID: 12073020 Review.
Hand-foot-genital syndrome (HFGS) is a dominantly inherited congenital malformation affecting the distal limbs and genitourinary tract. ...
Hand-foot-genital syndrome (HFGS) is a dominantly inherited congenital malformation affecting the distal limbs a …
12 results