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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

299 related items for PubMed ID: 24075385

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  • 26. Thanatophoric dysplasia (types I and II) caused by distinct mutations in fibroblast growth factor receptor 3.
    Tavormina PL, Shiang R, Thompson LM, Zhu YZ, Wilkin DJ, Lachman RS, Wilcox WR, Rimoin DL, Cohn DH, Wasmuth JJ.
    Nat Genet; 1995 Mar; 9(3):321-8. PubMed ID: 7773297
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  • 31. Thanatophoric dysplasia type 1 with cloverleaf skull in a dichorionic twin.
    Salinas-Torres VM.
    Genet Couns; 2015 Mar; 26(1):61-5. PubMed ID: 26043509
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  • 32. Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.
    Chen CP, Su YN, Chen YY, Chern SR, Liu YP, Wu PC, Lee CC, Chen YT, Wang W.
    Taiwan J Obstet Gynecol; 2011 Sep; 50(3):345-52. PubMed ID: 22030051
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  • 34. [Prenatal diagnosis of thanatophoric dysplasia at the 20th week of pregnancy using ultrasonography].
    Todros T, Sciarrone A, Voglino G, Botta G, Camera G.
    Pathologica; 1995 Dec; 87(6):723-5. PubMed ID: 8927442
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  • 37. FGFR3 mutation in thanatophoric dysplasia type 1 with bilateral cystic renal dysplasia: coincidence or a new association?
    Prontera P, Sensi A, Pilu G, Baldi M, Baffico M, Bonasoni R, Calzolari E.
    Genet Couns; 2006 Dec; 17(4):407-12. PubMed ID: 17375526
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