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 *

133 related articles for article (PubMed ID: 3515588)

  • 21. Genetic disorders in the Indian community of South Africa.
    Winship WS; Beighton P
    S Afr Med J; 2011 Jun; 101(7):481-4. PubMed ID: 21920103
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Pendred's syndrome in South African Bantu brothers.
    Levin SE; Klugman LH
    S Afr Med J; 1966 Aug; 40(32):759-60. PubMed ID: 4162049
    [No Abstract]   [Full Text] [Related]  

  • 23. Genetic disorders in Southern Africa.
    Beighton P
    S Afr Med J; 1976 Jul; 50(29):1125-8. PubMed ID: 959924
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Congenital contractural arachnodactyly in a black African kindred.
    Wainer S; Vos ET
    Cent Afr J Med; 1991 Aug; 37(8):262-4. PubMed ID: 1807801
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Pigmentary disorders in association with congenital deafness.
    Reed WB; Stone VM; Boder E; Ziprkowski L
    Arch Dermatol; 1967 Feb; 95(2):176-86. PubMed ID: 6018993
    [No Abstract]   [Full Text] [Related]  

  • 26. Genetics of deafness: clinical aspects.
    Reardon W
    Br J Hosp Med; 1992 Apr 1-14; 47(7):507-11. PubMed ID: 1581755
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Congenital and genetic disorders affecting the musculoskeletal system.
    Szer IS
    Curr Opin Rheumatol; 1989 Oct; 1(3):272-7. PubMed ID: 2701679
    [No Abstract]   [Full Text] [Related]  

  • 28. Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21.
    Tackels-Horne D; Toburen A; Sangiorgi E; Gurrieri F; de Mollerat X; Fischetto R; Causio F; Clarkson K; Stevenson RE; Schwartz CE
    Clin Genet; 2001 Jan; 59(1):28-36. PubMed ID: 11168022
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Studying prevalence of muscle-skeletal system and connective tissue among adult rural population of Lipetsk region].
    Shurshukov IuIu; Soldatova PF
    Med Tr Prom Ekol; 2007; (2):41-4. PubMed ID: 17436760
    [No Abstract]   [Full Text] [Related]  

  • 30. Hereditary deafness in man.
    Konigsmark BW
    N Engl J Med; 1969 Oct; 281(15):827-32 concl. PubMed ID: 4309240
    [No Abstract]   [Full Text] [Related]  

  • 31. Motor neuron disease in blacks. Epidemiological observations in Natal.
    Cosnett JE; Bill PL; Bhigjee AI
    S Afr Med J; 1989 Aug; 76(4):155-7. PubMed ID: 2762957
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3.
    Ignatius J; Knuutila S; Scherer SW; Trask B; Kere J
    J Med Genet; 1996 Jun; 33(6):507-10. PubMed ID: 8782053
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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; 41(5):e54. PubMed ID: 15121782
    [No Abstract]   [Full Text] [Related]  

  • 34. The foot and systemic disease in the Veterans Administration: a quantitation of the relationship between systemic disease and pedal problems.
    Port M; McCarthy DJ; Chu S
    J Am Podiatry Assoc; 1980 Aug; 70(8):397-404. PubMed ID: 7002981
    [No Abstract]   [Full Text] [Related]  

  • 35. Differentiation of heterozygotes in recessive albinism.
    Roberts DF; Kromberg JG; Jenkins T
    J Med Genet; 1986 Aug; 23(4):323-7. PubMed ID: 3091836
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ectrodactyly in central Africa.
    Viljoen D; Farrell HM; Brossy JJ; McArthur M; Maheswaran M; Beighton P
    S Afr Med J; 1985 Oct; 68(9):655-8. PubMed ID: 4060025
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Problem of pseudosyringomyelitic ulcerative-mutilating and deforming acropathy].
    Golemba PI; Guseva LL; Shakhnes IE
    Vestn Dermatol Venerol; 1973 Aug; 47(8):73-5. PubMed ID: 4767960
    [No Abstract]   [Full Text] [Related]  

  • 38. Population frequencies of inherited neuromuscular diseases--a world survey.
    Emery AE
    Neuromuscul Disord; 1991; 1(1):19-29. PubMed ID: 1822774
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Syndrome of imperforate anus, abnormalities of hands and feet, satyr ears, and sensorineural deafness.
    Walpole IR; Hockey A
    J Pediatr; 1982 Feb; 100(2):250-2. PubMed ID: 7199082
    [No Abstract]   [Full Text] [Related]  

  • 40. Osteochondrodysplasias in South Africa.
    Beighton P
    Am J Med Genet; 1996 May; 63(1):7-11. PubMed ID: 8723079
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.