BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

139 related articles for article (PubMed ID: 12885337)

  • 21. Connexin 26 gene mutation and autosomal recessive deafness.
    Reardon W
    Lancet; 1998 Feb; 351(9100):383-4. PubMed ID: 9482285
    [No Abstract]   [Full Text] [Related]  

  • 22. Genetic screening for deafness.
    Smith RJ; Hone S
    Pediatr Clin North Am; 2003 Apr; 50(2):315-29. PubMed ID: 12809325
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Causes of childhood deafness in Pukhtoonkhwa Province of Pakistan and the role of consanguinity.
    Sajjad M; Khattak AA; Bunn JE; Mackenzie I
    J Laryngol Otol; 2008 Oct; 122(10):1057-63. PubMed ID: 18423085
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Changing family structure in a modernizing society: a study of marriage patterns in a single Muslim village in Israel.
    Zlotogora J; Habiballa H; Odatalla A; Barges S
    Am J Hum Biol; 2002; 14(5):680-2. PubMed ID: 12203822
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A genetic aetiological survey of severe childhood deafness in the United Arab Emirates.
    Al-Gazali LI
    J Trop Pediatr; 1998 Jun; 44(3):157-60. PubMed ID: 9680781
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Marked parental consanguinity as a cause for increased major malformations in an Israeli Arab community.
    Jaber L; Merlob P; Bu X; Rotter JI; Shohat M
    Am J Med Genet; 1992 Sep; 44(1):1-6. PubMed ID: 1519638
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The association between consanguineous marriage and offspring with congenital hearing loss.
    Almazroua AM; Alsughayer L; Ababtain R; Al-Shawi Y; Hagr AA
    Ann Saudi Med; 2020; 40(6):456-461. PubMed ID: 33307738
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Consanguineous marriages in Morocco and the consequence for the incidence of autosomal recessive disorders.
    Jaouad IC; Elalaoui SC; Sbiti A; Elkerh F; Belmahi L; Sefiani A
    J Biosoc Sci; 2009 Sep; 41(5):575-81. PubMed ID: 19433002
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic disorders among Palestinian Arabs. 4: Genetic clinics in the community.
    Zlotogora J; Barges S; Bisharat B; Shalev SA
    Am J Med Genet A; 2006 Aug; 140(15):1644-6. PubMed ID: 16830330
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [From gene to disease: deafness and connexin 26].
    Hoefsloot LH; Kemperman M; Cremers CW
    Ned Tijdschr Geneeskd; 2002 Feb; 146(6):259-61. PubMed ID: 11865655
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Deafness genes in Israel: implications for diagnostics in the clinic.
    Brownstein Z; Avraham KB
    Pediatr Res; 2009 Aug; 66(2):128-34. PubMed ID: 19390476
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic disorders among Palestinian Arabs: 3. Autosomal recessive disorders in a single village.
    Zlotogora J; Shalev S; Habiballah H; Barjes S
    Am J Med Genet; 2000 Jun; 92(5):343-5. PubMed ID: 10861664
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart.
    Arnos KS; Welch KO; Tekin M; Norris VW; Blanton SH; Pandya A; Nance WE
    Am J Hum Genet; 2008 Aug; 83(2):200-7. PubMed ID: 18656178
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Connexin 26 mutations: the first practical genetic marker of inherited hearing loss.
    Perry CF
    Med J Aust; 2001 Aug; 175(4):182-3. PubMed ID: 11587274
    [No Abstract]   [Full Text] [Related]  

  • 35. Impact of genetic counseling and Connexin-26 and Connexin-30 testing on deaf identity and comprehension of genetic test results in a sample of deaf adults: a prospective, longitudinal study.
    Palmer CG; Boudreault P; Baldwin EE; Sinsheimer JS
    PLoS One; 2014; 9(11):e111512. PubMed ID: 25375116
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Autosomal recessive nonsyndromal profound childhood deafness in a large pedigree. Audiometric features of the affected persons and the obligate carriers.
    Marres HA; Cremers CW
    Arch Otolaryngol Head Neck Surg; 1989 May; 115(5):591-5. PubMed ID: 2706105
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutation screening for deafness: more than simply another diagnostic test.
    Smith RJ
    Arch Otolaryngol Head Neck Surg; 2001 Aug; 127(8):941-2. PubMed ID: 11493202
    [No Abstract]   [Full Text] [Related]  

  • 38. Genetics of deafness in India.
    Ghosh M; Vijaya R; Kabra M
    Indian J Pediatr; 2004 Jun; 71(6):531-3. PubMed ID: 15226564
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village.
    Winata S; Arhya IN; Moeljopawiro S; Hinnant JT; Liang Y; Friedman TB; Asher JH
    J Med Genet; 1995 May; 32(5):336-43. PubMed ID: 7616538
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Decline in the prevalence of childhood deafness in the Jewish population of Jerusalem: ethnic and genetic aspects.
    Feinmesser M; Tell L; Levi H
    J Laryngol Otol; 1990 Sep; 104(9):675-7. PubMed ID: 2230571
    [TBL] [Abstract][Full Text] [Related]  

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