PubMed (OMIM) for id: 401304

Year	Number of Results
1970	1
1989	2
1992	1
1993	1
1996	1
1997	1
2000	1
2002	3
2024	0

1

Severe digital abnormalities in a patient heterozygous for both a novel missense mutation in HOXD13 and a polyalanine tract expansion in HOXA13.

Debeer P, Bacchelli C, Scambler PJ, De Smet L, Fryns JP, Goodman FR. Debeer P, et al. J Med Genet. 2002 Nov;39(11):852-6. doi: 10.1136/jmg.39.11.852. J Med Genet. 2002. PMID: 12414828 Free PMC article. No abstract available.

2

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.

3

A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.

Innis JW, Goodman FR, Bacchelli C, Williams TM, Mortlock DP, Sateesh P, Scambler PJ, McKinnon W, Guttmacher AE. Innis JW, et al. Hum Mutat. 2002 May;19(5):573-4. doi: 10.1002/humu.9036. Hum Mutat. 2002. PMID: 11968094 Free article.

4

Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.

Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Goodman FR, et al. Am J Hum Genet. 2000 Jul;67(1):197-202. doi: 10.1086/302961. Epub 2000 Jun 5. Am J Hum Genet. 2000. PMID: 10839976 Free PMC article.

5

Mutation of HOXA13 in hand-foot-genital syndrome.

Mortlock DP, Innis JW. Mortlock DP, et al. Nat Genet. 1997 Feb;15(2):179-80. doi: 10.1038/ng0297-179. Nat Genet. 1997. PMID: 9020844

6

The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation.

Mortlock DP, Post LC, Innis JW. Mortlock DP, et al. Nat Genet. 1996 Jul;13(3):284-9. doi: 10.1038/ng0796-284. Nat Genet. 1996. PMID: 8673126

7

Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.

Guttmacher AE. Guttmacher AE. Am J Med Genet. 1993 Apr 15;46(2):219-22. doi: 10.1002/ajmg.1320460223. Am J Med Genet. 1993. PMID: 8484413

8

The hand-food-uterus syndrome: a new hereditary disorder characterized by hand and foot dysplasia, dermatoglyphic abnormalities, and partial duplication of the female genital tract.

Stern AM, Gall JC Jr, Perry BL, Stimson CW, Weitkamp LR, Poznanski AK. Stern AM, et al. J Pediatr. 1970 Jul;77(1):109-16. doi: 10.1016/s0022-3476(70)80052-x. J Pediatr. 1970. PMID: 5450271 No abstract available.

9

Urinary tract abnormalities in hand-foot-genital syndrome.

Verp MS. Verp MS. Am J Med Genet. 1989 Apr;32(4):555. doi: 10.1002/ajmg.1320320429. Am J Med Genet. 1989. PMID: 2774004 No abstract available.

10

The human HOX gene family.

Acampora D, D'Esposito M, Faiella A, Pannese M, Migliaccio E, Morelli F, Stornaiuolo A, Nigro V, Simeone A, Boncinelli E. Acampora D, et al. Nucleic Acids Res. 1989 Dec 25;17(24):10385-402. doi: 10.1093/nar/17.24.10385. Nucleic Acids Res. 1989. PMID: 2574852 Free PMC article.

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