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 *

170 related articles for article (PubMed ID: 9063741)

  • 1. Homozygosity mapping at Alström syndrome to chromosome 2p.
    Collin GB; Marshall JD; Cardon LR; Nishina PM
    Hum Mol Genet; 1997 Feb; 6(2):213-9. PubMed ID: 9063741
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Refinement of genetic localization of the Alström syndrome on chromosome 2p12-13 by linkage analysis in a North African family.
    Macari F; Lautier C; Girardet A; Dadoun F; Darmon P; Dutour A; Renard E; Bouvagnet P; Claustres M; Oliver C; Grigorescu F
    Hum Genet; 1998 Dec; 103(6):658-61. PubMed ID: 9921899
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Alström syndrome: further evidence for linkage to human chromosome 2p13.
    Collin GB; Marshall JD; Boerkoel CF; Levin AV; Weksberg R; Greenberg J; Michaud JL; Naggert JK; Nishina PM
    Hum Genet; 1999 Nov; 105(5):474-9. PubMed ID: 10598815
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Three new cases of Alström syndrome.
    Benso C; Hadjadj E; Conrath J; Denis D
    Graefes Arch Clin Exp Ophthalmol; 2002 Aug; 240(8):622-7. PubMed ID: 12192455
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genealogy, natural history, and phenotype of Alström syndrome in a large Acadian kindred and three additional families.
    Marshall JD; Ludman MD; Shea SE; Salisbury SR; Willi SM; LaRoche RG; Nishina PM
    Am J Med Genet; 1997 Dec; 73(2):150-61. PubMed ID: 9409865
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Alström syndrome: is it a rare or unknown disease?
    Maffei P; Munno V; Marshall JD; Scandellari C; Sicolo N
    Ann Ital Med Int; 2002; 17(4):221-8. PubMed ID: 12532560
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Alström syndrome: clinical and genetic features, and a diagnostic guide to foresee complications].
    Mendioroz J; Bermejo E; Marshall JD; Naggert JK; Collin GB; Martínez-Frías ML
    Med Clin (Barc); 2008 Nov; 131(19):741-6. PubMed ID: 19091203
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36.
    Lubianca Neto JF; Lu L; Eavey RD; Flores MA; Caldera RM; Sangwatanaroj S; Schott JJ; McDonough B; Santos JI; Seidman CE; Seidman JG
    Am J Hum Genet; 1998 May; 62(5):1107-12. PubMed ID: 9545407
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Homozygosity mapping of achromatopsia to chromosome 2 using DNA pooling.
    Arbour NC; Zlotogora J; Knowlton RG; Merin S; Rosenmann A; Kanis AB; Rokhlina T; Stone EM; Sheffield VC
    Hum Mol Genet; 1997 May; 6(5):689-94. PubMed ID: 9158143
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Alstrom syndrome: confirmation of linkage to chromosome 2p12-13 and phenotypic heterogeneity in three affected sibs.
    Zumsteg U; Muller PY; Miserez AR
    J Med Genet; 2000 Jul; 37(7):E8. PubMed ID: 10882760
    [No Abstract]   [Full Text] [Related]  

  • 11. Alstrom syndrome in four sibs from northern Jordan.
    Hamamy H; Barham M; Alkhawaldeh AE; Cockburn D; Snowden H; Ajlouni K
    Ann Saudi Med; 2006; 26(6):480-3. PubMed ID: 17146208
    [No Abstract]   [Full Text] [Related]  

  • 12. Characterization of the murine Lbx2 promoter, identification of the human homologue, and evaluation as a candidate for Alström syndrome.
    Chen F; Collin GB; Liu KC; Beier DR; Eccles M; Nishina PM; Moshang T; Epstein JA
    Genomics; 2001 Jun; 74(2):219-27. PubMed ID: 11386758
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness.
    Moynihan LM; Bundey SE; Heath D; Jones EL; McHale DP; Mueller RF; Markham AF; Lench NJ
    Am J Hum Genet; 1998 May; 62(5):1123-8. PubMed ID: 9545394
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Long-term clinical follow-up and molecular testing for diagnosis of the first Tunisian family with Alström syndrome.
    Chakroun A; Ben Said M; Ennouri A; Achour I; Mnif M; Abid M; Ghorbel A; Marshall JD; Naggert JK; Masmoudi S
    Eur J Med Genet; 2016 Sep; 59(9):444-51. PubMed ID: 27523285
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Acute lymphoblastic leukemia in one of two siblings with Alstrom syndrome.
    Chen BH; Chiou SS; Tsai RK; Lin YF; Wu JR
    J Formos Med Assoc; 2000 Oct; 99(10):792-5. PubMed ID: 11061078
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Human DCTN1: genomic structure and evaluation as a candidate for Alström syndrome.
    Collin GB; Nishina PM; Marshall JD; Naggert JK
    Genomics; 1998 Nov; 53(3):359-64. PubMed ID: 9799602
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DFNB39, a recessive form of sensorineural hearing impairment, maps to chromosome 7q11.22-q21.12.
    Wajid M; Abbasi AA; Ansar M; Pham TL; Yan K; Haque S; Ahmad W; Leal SM
    Eur J Hum Genet; 2003 Oct; 11(10):812-5. PubMed ID: 14512973
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.
    Ruf RG; Wolf MT; Hennies HC; Lucke B; Zinn C; Varnholt V; Lichtenberger A; Pasch A; Imm A; Briese S; Lennert T; Fuchshuber A; Nurnberg P; Hildebrandt F
    J Am Soc Nephrol; 2003 Jun; 14(6):1519-22. PubMed ID: 12761252
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alström syndrome with subclinical insulin-resistant diabetes and hepatic dysfunction: a family report.
    Chou PI; Chen CH; Chen JT; Wen LY; Wu DA; Feldon SE
    J Pediatr Ophthalmol Strabismus; 2000; 37(3):179-82. PubMed ID: 10845422
    [No Abstract]   [Full Text] [Related]  

  • 20. Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity.
    Kwitek-Black AE; Carmi R; Duyk GM; Buetow KH; Elbedour K; Parvari R; Yandava CN; Stone EM; Sheffield VC
    Nat Genet; 1993 Dec; 5(4):392-6. PubMed ID: 8298649
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.