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PUBMED FOR HANDHELDS

Journal Abstract Search


216 related items for PubMed ID: 31633898

  • 21.
    ; . PubMed ID:
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  • 22.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Mehta PA, Ebens C.
    ; 1993. PubMed ID: 20301575
    [Abstract] [Full Text] [Related]

  • 23. Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic COL10A1 variant.
    Ain NU, Makitie O, Naz S.
    J Med Genet; 2018 Jun; 55(6):403-407. PubMed ID: 28830906
    [Abstract] [Full Text] [Related]

  • 24.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Wallace SE, Wilcox WR.
    ; 1993 Jun. PubMed ID: 20301335
    [Abstract] [Full Text] [Related]

  • 25.
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  • 26. A novel COL10A1 mutation in a Chinese pedigree with Schmid type metaphyseal chondrodysplasia.
    Hu X, Zhang X, Li Y, Lou P, Li X, Jiang L.
    Clin Lab; 2015 Jun; 61(3-4):227-33. PubMed ID: 25974987
    [Abstract] [Full Text] [Related]

  • 27.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Briggs MD, Wright MJ.
    ; 1993 Jun. PubMed ID: 20301660
    [Abstract] [Full Text] [Related]

  • 28.
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  • 30.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Regier DS, Tifft CJ, Rothermel CE.
    ; 1993 Jun. PubMed ID: 24156116
    [Abstract] [Full Text] [Related]

  • 31.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Steiner RD, Basel D.
    ; 1993 Jun. PubMed ID: 20301472
    [Abstract] [Full Text] [Related]

  • 32. A novel missense COL10A1 mutation: c.2020G>A; p. Gly674Arg linked with the bowed legs stature in the Schmid metaphyseal chondrodysplasia-affected Chinese lineage.
    Chen Q, Wu SN, Chen YX, C SK, Zhang L, Wei HY, Kumar SA.
    Bone Rep; 2020 Jun; 12():100240. PubMed ID: 31921940
    [Abstract] [Full Text] [Related]

  • 33.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Bhavani GS, Singh S, Girisha KM.
    ; 1993 Jun. PubMed ID: 37229238
    [Abstract] [Full Text] [Related]

  • 34.
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  • 35. Identification of four novel COL10A1 missense mutations in schmid metaphyseal chondrodysplasia: further evidence that collagen X NC1 mutations impair trimer assembly.
    Bateman JF, Freddi S, McNeil R, Thompson E, Hermanns P, Savarirayan R, Lamandé SR.
    Hum Mutat; 2004 Apr; 23(4):396. PubMed ID: 15024737
    [Abstract] [Full Text] [Related]

  • 36.
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  • 37. A Novel Presentation of Metaphyseal Chondrodysplasia, Schmid Type with Factor VII Deficiency.
    Ahmed M, Nasir S, Riaz Hashmi SS, Iqbal Z, Saleem A.
    Cureus; 2020 Mar 23; 12(3):e7371. PubMed ID: 32328382
    [Abstract] [Full Text] [Related]

  • 38.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Robertson S.
    ; 1993 Mar 23. PubMed ID: 20301567
    [Abstract] [Full Text] [Related]

  • 39.
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  • 40.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Angelini C.
    ; 1993 Mar 23. PubMed ID: 20301490
    [Abstract] [Full Text] [Related]


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