148 related articles for article (PubMed ID: 9072822)
1. HOX gene links limb, genital defects.
Dickman S
Science; 1997 Mar; 275(5306):1568. PubMed ID: 9072822
[No Abstract] [Full Text] [Related]
2. Human HOX gene mutations.
Goodman FR; Scambler PJ
Clin Genet; 2001 Jan; 59(1):1-11. PubMed ID: 11206481
[TBL] [Abstract][Full Text] [Related]
3. 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
Am J Hum Genet; 2000 Jul; 67(1):197-202. PubMed ID: 10839976
[TBL] [Abstract][Full Text] [Related]
4. Mirror hands and feet.
van Steensel MA
J Med Genet; 1997 Aug; 34(8):701-2. PubMed ID: 9279770
[No Abstract] [Full Text] [Related]
5. Mutation of HOXA13 in hand-foot-genital syndrome.
Mortlock DP; Innis JW
Nat Genet; 1997 Feb; 15(2):179-80. PubMed ID: 9020844
[TBL] [Abstract][Full Text] [Related]
6. Triphalangeal thumbs with brachyectrodactyly: a sporadic case.
Brown AM; Romness M; Dong DA; Kelly TE
Am J Med Genet A; 2008 Nov; 146A(21):2835-6. PubMed ID: 18924168
[No Abstract] [Full Text] [Related]
7. [Hand-foot-genital syndrome].
Mitsubuchi H; Endo F
Nihon Rinsho; 2006 Jun; Suppl 2():647-8. PubMed ID: 16817484
[No Abstract] [Full Text] [Related]
8. Multifaceted Hoxa13 function in urogenital development underlies the Hand-Foot-Genital Syndrome.
Roux M; Bouchard M; Kmita M
Hum Mol Genet; 2019 May; 28(10):1671-1681. PubMed ID: 30649340
[TBL] [Abstract][Full Text] [Related]
9. Hallux valgus interphalangeus and a novel mutation in HOXA13. Part of the broadening spectrum of Hand-Foot-Genital syndrome.
Parker L; Mangwani J; Wakeling E; Singh D
Foot Ankle Surg; 2011 Jun; 17(2):e28-30. PubMed ID: 21549968
[TBL] [Abstract][Full Text] [Related]
10. Limb malformations and the human HOX genes.
Goodman FR
Am J Med Genet; 2002 Oct; 112(3):256-65. PubMed ID: 12357469
[TBL] [Abstract][Full Text] [Related]
11. A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family.
Cao L; Chen C; Leng Y; Yan L; Wang S; Zhang X; Luo Y
J Genet; 2017 Sep; 96(4):647-652. PubMed ID: 28947713
[TBL] [Abstract][Full Text] [Related]
12. Dual genetic diagnoses: Atypical hand-foot-genital syndrome and developmental delay due to de novo mutations in HOXA13 and NRXN1.
Wallis M; Tsurusaki Y; Burgess T; Borzi P; Matsumoto N; Miyake N; True D; Patel C
Am J Med Genet A; 2016 Mar; 170(3):717-24. PubMed ID: 26590955
[TBL] [Abstract][Full Text] [Related]
13. 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
Hum Mutat; 2002 May; 19(5):573-4. PubMed ID: 11968094
[TBL] [Abstract][Full Text] [Related]
14. Hand-foot-genital syndrome - analysis of two cases.
Piazza MJ; Urbanetz AA
JBRA Assist Reprod; 2018 Jun; 22(2):157-159. PubMed ID: 29638102
[TBL] [Abstract][Full Text] [Related]
15. Hand-foot-genital syndrome: the importance of hallux varus.
Cleveland RH; Holmes LB
Pediatr Radiol; 1990; 20(5):339-43. PubMed ID: 2349017
[TBL] [Abstract][Full Text] [Related]
16. Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.
Tas E; Sebastian J; Madan-Khetarpal S; Sweet P; Yatsenko AN; Pollock N; Rajkovic A; Schneck FX; Yatsenko SA; Witchel SF
Am J Med Genet A; 2017 Jan; 173(1):221-224. PubMed ID: 27649277
[TBL] [Abstract][Full Text] [Related]
17. Hand-foot-genital syndrome with a 7p15 deletion: clinically recognizable syndrome.
Hosoki K; Ohta T; Fujita K; Nishigaki S; Shiomi M; Niikawa N; Saitoh S
Pediatr Int; 2012 Jun; 54(3):e22-5. PubMed ID: 22631585
[No Abstract] [Full Text] [Related]
18. Al-Awadi-Raas-Rothschild (limb/pelvis/uterus-hypoplasia/aplasia) syndrome and WNT7A mutations: genetic homogeneity and nosological delineation.
Garavelli L; Wischmeijer A; Rosato S; Gelmini C; Reverberi S; Sassi S; Ferrari A; Mari F; Zabel B; Lausch E; Unger S; Superti-Furga A
Am J Med Genet A; 2011 Feb; 155A(2):332-6. PubMed ID: 21271649
[No Abstract] [Full Text] [Related]
19. The hand-foot-genital syndrome: on the variable expression in affected males.
Fryns JP; Vogels A; Decock P; van den Berghe H
Clin Genet; 1993 May; 43(5):232-4. PubMed ID: 8375102
[TBL] [Abstract][Full Text] [Related]
20. Severe manifestations of hand-foot-genital syndrome associated with a novel HOXA13 mutation.
Imagawa E; Kayserili H; Nishimura G; Nakashima M; Tsurusaki Y; Saitsu H; Ikegawa S; Matsumoto N; Miyake N
Am J Med Genet A; 2014 Sep; 164A(9):2398-402. PubMed ID: 24934387
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
