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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

80 related articles for article (PubMed ID: 6819575)

  • 1. Classic X-linked spondyloepiphyseal dysplasia tarda in a woman with normal karyotype.
    Monteiro de Pina Neto J; Bonfim MD; Ferrari I
    Prog Clin Biol Res; 1982; 104():127-32. PubMed ID: 6819575
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Spondyloepiphyseal dysplasia tarda (X-linked recessive form)].
    Søgaard HJ; Aagaard VE
    Ugeskr Laeger; 1981 May; 143(19):1219-20. PubMed ID: 6795778
    [No Abstract]   [Full Text] [Related]  

  • 3. Spondyloepiphyseal dysplasia tarda, X-linked form.
    Lie SO
    Birth Defects Orig Artic Ser; 1974; 10(12):383-6. PubMed ID: 4218777
    [No Abstract]   [Full Text] [Related]  

  • 4. X-linked spondyloepiphyseal dysplasia tarda: clinical and linkage data.
    Bannerman RM; Ingall GB; Mohn JF
    J Med Genet; 1971 Sep; 8(3):291-301. PubMed ID: 4999590
    [No Abstract]   [Full Text] [Related]  

  • 5. X-linked spondyloepiphyseal dysplasia tarda: mucopolysaccharide excretion studies.
    Thompson GR; Thompson DE; McCann DS; Weiss JJ
    Clin Rheumatol; 1982 Dec; 1(4):281-4. PubMed ID: 6821378
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Identification of a novel mutation IVS2-2A-->C of SEDL gene in a Chinese family with X-linked spondyloepiphyseal dysplasia tarda].
    Gao C; Luo Q; Wang HL; Gao XQ; Fan QT; Wang H; Sheng GY; Zhou JH; Gao TZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Feb; 20(1):15-8. PubMed ID: 12579492
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two first cousins with spondyloepiphyseal dysplasia tarda (X linked recessive form), one also with poikiloderma atrophicans vasculare progressing to lymphocytic lymphoma.
    Branford WA; Beveridge GW; Wynne-Davies R
    J Med Genet; 1982 Jun; 19(3):210-3. PubMed ID: 6809944
    [TBL] [Abstract][Full Text] [Related]  

  • 8. X-linked mental retardation: Renpenning revisited.
    Fox P; Fox D; Gerrard JW
    Am J Med Genet; 1980; 7(4):491-5. PubMed ID: 7211958
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Mutational analysis in a family with X-linked spondyloepiphyseal dysplasia tarda].
    Zhu HY; Li J; Zhu RF; Wu X; Duan HL; Yang Y; Zhang Y; Hu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):421-3. PubMed ID: 18683141
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda.
    Gedeon AK; Colley A; Jamieson R; Thompson EM; Rogers J; Sillence D; Tiller GE; Mulley JC; Gécz J
    Nat Genet; 1999 Aug; 22(4):400-4. PubMed ID: 10431248
    [TBL] [Abstract][Full Text] [Related]  

  • 11. X-linked mental retardation with macro-orchidism and marker-X chromosomes.
    Martin RH; Lin CC; Mathies BJ; Lowry RB
    Am J Med Genet; 1980; 7(4):433-41. PubMed ID: 6938132
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-linked spondyloepiphyseal dysplasia tarda: Novel and recurrent mutations in 13 European families.
    Fiedler J; Le Merrer M; Mortier G; Heuertz S; Faivre L; Brenner RE
    Hum Mutat; 2004 Jul; 24(1):103. PubMed ID: 15221797
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Twin pregnancy in woman with 45,X/47,XXX karyotype.
    Kivinen S; Herva R
    Obstet Gynecol; 1980 Sep; 56(3):401-2. PubMed ID: 7422184
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic heterogeneity in spondyloepiphyseal dysplasia congenita.
    Harrod MJ; Friedman JM; Currarino G; Pauli RM; Langer LO
    Am J Med Genet; 1984 Jun; 18(2):311-20. PubMed ID: 6431817
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization].
    Huang Y; Sun X; Li Q
    Zhonghua Yi Xue Za Zhi; 1999 Feb; 79(2):106-8. PubMed ID: 11601014
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Opitz GBBB syndrome: chromosomal evidence of an X-linked form.
    Verloes A; David A; Odent S; Toutain A; André MJ; Lucas J; Le Marec B
    Am J Med Genet; 1995 Oct; 59(1):123-8. PubMed ID: 8849003
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X-linked mental retardation: a study of 7 families.
    Jacobs PA; Glover TW; Mayer M; Fox P; Gerrard JW; Dunn HG; Herbst DS
    Am J Med Genet; 1980; 7(4):471-89. PubMed ID: 7211957
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Skewed X-chromosome inactivation causes intra-familial phenotypic variation of an EBP mutation in a family with X-linked dominant chondrodysplasia punctata.
    Shirahama S; Miyahara A; Kitoh H; Honda A; Kawase A; Yamada K; Mabuchi A; Kura H; Yokoyama Y; Tsutsumi M; Ikeda T; Tanaka N; Nishimura G; Ohashi H; Ikegawa S
    Hum Genet; 2003 Jan; 112(1):78-83. PubMed ID: 12483303
    [TBL] [Abstract][Full Text] [Related]  

  • 19. X-linked chronic granulomatous disease in an adult woman. Evidence for a cell selection favoring neutrophils expressing the mutant allele.
    Cazzola M; Sacchi F; Pagani A; Marconi M; Ciriello MM; Fietta A; Clivio A; Ascari E
    Haematologica; 1985; 70(4):291-5. PubMed ID: 3935525
    [No Abstract]   [Full Text] [Related]  

  • 20. Spondyloepiphyseal dysplasia tarda with progressive arthropathy.
    Al-Awadi SA; Fårag TI; Naguib K; El-Khalifa MY; Cuschieri A; Hosny G; Zahran M; Al-Ansari AG
    J Med Genet; 1984 Jun; 21(3):193-6. PubMed ID: 6431106
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.