These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

203 related items for PubMed ID: 29638102

  • 1. Hand-foot-genital syndrome - analysis of two cases.
    Piazza MJ, Urbanetz AA.
    JBRA Assist Reprod; 2018 Jun 01; 22(2):157-159. PubMed ID: 29638102
    [Abstract] [Full Text] [Related]

  • 2. 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 01; 173(1):221-224. PubMed ID: 27649277
    [Abstract] [Full Text] [Related]

  • 3. 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 01; 96(4):647-652. PubMed ID: 28947713
    [Abstract] [Full Text] [Related]

  • 4. [Hand-foot-genital syndrome].
    Mitsubuchi H, Endo F.
    Nihon Rinsho; 2006 Jun 28; Suppl 2():647-8. PubMed ID: 16817484
    [No Abstract] [Full Text] [Related]

  • 5. B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?
    Edery P, Le Deist F, Briard ML, Debré M, Munnich A, Griscelli C, Fischer A, Lyonnet S.
    J Med Genet; 2001 Jul 28; 38(7):488-93. PubMed ID: 11476068
    [No Abstract] [Full Text] [Related]

  • 6. 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 28; 54(3):e22-5. PubMed ID: 22631585
    [No Abstract] [Full Text] [Related]

  • 7. 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 28; 170(3):717-24. PubMed ID: 26590955
    [Abstract] [Full Text] [Related]

  • 8. 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 28; 164A(9):2398-402. PubMed ID: 24934387
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies.
    Jorgensen EM, Ruman JI, Doherty L, Taylor HS.
    Fertil Steril; 2010 Sep 28; 94(4):1235-1238. PubMed ID: 19591980
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Multifaceted Hoxa13 function in urogenital development underlies the Hand-Foot-Genital Syndrome.
    Roux M, Bouchard M, Kmita M.
    Hum Mol Genet; 2019 May 15; 28(10):1671-1681. PubMed ID: 30649340
    [Abstract] [Full Text] [Related]

  • 15. [The hand-foot-uterus syndrome. A report of a case with recessive autosomal inheritance].
    Stella NC, Triolo O, Corrado F.
    Minerva Ginecol; 1993 Sep 15; 45(9):429-32. PubMed ID: 8255504
    [Abstract] [Full Text] [Related]

  • 16. Analysis of de novo HOXA13 polyalanine expansions supports replication slippage without repair in their generation.
    Owens KM, Quinonez SC, Thomas PE, Keegan CE, Lefebvre N, Roulston D, Larsen CA, Stadler HS, Innis JW.
    Am J Med Genet A; 2013 May 15; 161A(5):1019-27. PubMed ID: 23532960
    [Abstract] [Full Text] [Related]

  • 17. Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia.
    Wieland I, Muschke P, Jakubiczka S, Volleth M, Freigang B, Wieacker PF.
    J Med Genet; 2004 May 15; 41(5):e54. PubMed ID: 15121782
    [No Abstract] [Full Text] [Related]

  • 18. Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance.
    Mansour S, Swinkels M, Terhal PA, Wilson LC, Rich P, Van Maldergem L, Zwijnenburg PJ, Hall CM, Robertson SP, Newbury-Ecob R.
    Eur J Hum Genet; 2012 Oct 15; 20(10):1024-31. PubMed ID: 22473091
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.