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 *

95 related articles for article (PubMed ID: 1415339)

  • 21. Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case.
    Ng YY; Hu JM; Su PH; Chen JY; Yang MS; Chen SJ
    Acta Paediatr Taiwan; 2006; 47(3):142-5. PubMed ID: 17078468
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetic epidemiology of visceral leishmaniasis in northeastern Brazil.
    Peacock CS; Collins A; Shaw MA; Silveira F; Costa J; Coste CH; Nascimento MD; Siddiqui R; Shaw JJ; Blackwell JM
    Genet Epidemiol; 2001 Apr; 20(3):383-96. PubMed ID: 11255246
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Segregation analysis of alcoholism in high density families: a replication.
    Yuan H; Marazita ML; Hill SY
    Am J Med Genet; 1996 Feb; 67(1):71-6. PubMed ID: 8678118
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Autosomal dominant Goldenhar syndrome.
    Godel V; Regenbogen L; Goya V; Goodman RM
    Birth Defects Orig Artic Ser; 1982; 18(6):621-8. PubMed ID: 7171780
    [No Abstract]   [Full Text] [Related]  

  • 25. Complex segregation analysis of antibodies to thyroid peroxidase in Old Order Amish families.
    Pauls DL; Zakarija M; McKenzie JM; Egeland JA
    Am J Med Genet; 1993 Sep; 47(3):375-9. PubMed ID: 8135284
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Segregation analysis of cutaneous melanoma in Queensland.
    Aitken JF; Bailey-Wilson J; Green AC; MacLennan R; Martin NG
    Genet Epidemiol; 1998; 15(4):391-401. PubMed ID: 9671988
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Familial high myopia: evidence of an autosomal dominant mode of inheritance and genetic heterogeneity.
    Naiglin L; Clayton J; Gazagne C; Dallongeville F; Malecaze F; Calvas P
    Ann Genet; 1999; 42(3):140-6. PubMed ID: 10526656
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Mode of inheritance of idiopathic generalized non-myoclonic epilepsy in families investigated by studying members with idiopathic epilepsy with tonic-clonic crises on waking. Antioquia, Colombia].
    Mora O; Jiménez I; Palacio LG; Jiménez M; Sánchez JL; Zuluaga L; Uribe CS; Isaza R; Muñoz A; Arcos-Burgos M
    Rev Neurol; 1999 Apr 16-30; 28(8):768-71. PubMed ID: 10363319
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A genetic study of hypoalphalipoproteinemia.
    Byard PJ; Borecki IB; Glueck CJ; Laskarzewski PM; Third JL; Rao DC
    Genet Epidemiol; 1984; 1(1):43-51. PubMed ID: 6544231
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Inheritance of idiopathic torsion dystonia among Ashkenazi Jews.
    Bressman SB; de Leon D; Brin MF; Risch N; Shale H; Burke RE; Greene PE; Fahn S
    Adv Neurol; 1988; 50():45-56. PubMed ID: 3400502
    [TBL] [Abstract][Full Text] [Related]  

  • 31. New segregation analysis of panic disorder.
    Vieland VJ; Goodman DW; Chapman T; Fyer AJ
    Am J Med Genet; 1996 Apr; 67(2):147-53. PubMed ID: 8723041
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Autosomal dominant oculoauriculovertebral spectrum and 14q23.1 microduplication.
    Ballesta-Martínez MJ; López-González V; Dulcet LA; Rodríguez-Santiago B; Garcia-Miñaúr S; Guillen-Navarro E
    Am J Med Genet A; 2013 Aug; 161A(8):2030-5. PubMed ID: 23794319
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Power of segregation analysis for detection of major gene effects on quantitative traits.
    Borecki IB; Province MA; Rao DC
    Genet Epidemiol; 1994; 11(5):409-18. PubMed ID: 7835687
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Segregation analysis of leprosy in families of northern Thailand.
    Wagener DK; Schauf V; Nelson KE; Scollard D; Brown A; Smith T
    Genet Epidemiol; 1988; 5(2):95-105. PubMed ID: 3402727
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Segregation analyses of four urinary caffeine metabolite ratios implicated in the determination of human acetylation phenotypes.
    Vincent-Viry M; Pontes ZB; Gueguen R; Galteau MM; Siest G
    Genet Epidemiol; 1994; 11(2):115-29. PubMed ID: 8013893
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Segregation analysis of juvenile myoclonic epilepsy.
    Greenberg DA; Delgado-Escueta AV; Maldonado HM; Widelitz H
    Genet Epidemiol; 1988; 5(2):81-94. PubMed ID: 3136050
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Further evidence for an autosomal dominant form of oculoauriculovertebral dysplasia.
    Regenbogen L; Godel V; Goya V; Goodman RM
    Clin Genet; 1982 Mar; 21(3):161-7. PubMed ID: 7094392
    [No Abstract]   [Full Text] [Related]  

  • 38. Genetic influences in autism.
    Smalley SL
    Psychiatr Clin North Am; 1991 Mar; 14(1):125-39. PubMed ID: 2047327
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism.
    Ritvo ER; Spence MA; Freeman BJ; Mason-Brothers A; Mo A; Marazita ML
    Am J Psychiatry; 1985 Feb; 142(2):187-92. PubMed ID: 4038589
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 31 cases with oculoauriculovertebral dysplasia (Goldenhar syndrome): clinical, neuroradiologic, audiologic and cytogenetic findings.
    Engiz O; Balci S; Unsal M; Ozer S; Oguz KK; Aktas D
    Genet Couns; 2007; 18(3):277-88. PubMed ID: 18019368
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.