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 *

89 related articles for article (PubMed ID: 7470271)

  • 1. [Hypermethioninemia. Apropos of a case in a consanguineous couple].
    Guízar Vázquez J; Sánchez Aguilar G; Velázquez A; Fragoso R; Rostenberg I; Alejandre I
    Bol Med Hosp Infant Mex; 1980; 37(6):1237-44. PubMed ID: 7470271
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital vocal cord paralysis with possible autosomal recessive inheritance: case report and review of the literature.
    Koppel R; Friedman S; Fallet S
    Am J Med Genet; 1996 Aug; 64(3):485-7. PubMed ID: 8862626
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cutis laxa of the autosomal recessive type in a consanguineous family.
    de Schepper S; Loeys B; de Paepe A; Lambert J; Naeyaert JM
    Eur J Dermatol; 2003; 13(6):529-33. PubMed ID: 14721770
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chylous ascites in sibs from a consanguineous marriage.
    Flores S; Leungas J; Arredondo-Vega F; Guízar-Vázquez J
    Am J Med Genet; 1979; 3(2):145-8. PubMed ID: 474627
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Uncomplicated familial hypospadias: evidence for autosomal recessive inheritance.
    Frydman M; Greiber C; Cohen HA
    Am J Med Genet; 1985 May; 21(1):51-60. PubMed ID: 4003448
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Alopecia universalis as a single abnormality in an inbred Pakistani kindred.
    Ahmad M; Abbas H; Haque S
    Am J Med Genet; 1993 Jun; 46(4):369-71. PubMed ID: 8357006
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E; Palmieri A; Bertola A; Bellini C
    Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cleft lip and cone-rod dystrophy in a consanguineous sibship.
    Ausems MG; Wittebol-Post D; Hennekam RC
    Clin Dysmorphol; 1996 Oct; 5(4):307-11. PubMed ID: 8905195
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Setleis syndrome: autosomal recessive or autosomal dominant inheritance?
    al-Gazali LI; al-Talabani J
    Clin Dysmorphol; 1996 Jul; 5(3):249-53. PubMed ID: 8818454
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Consanguinity and deafness in Omani children.
    Khabori MA; Patton MA
    Int J Audiol; 2008 Jan; 47(1):30-3. PubMed ID: 18196484
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal recessive primary generalized dystonia in two siblings from a consanguineous family.
    Moretti P; Hedera P; Wald J; Fink J
    Mov Disord; 2005 Feb; 20(2):245-7. PubMed ID: 15390074
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Truncus arteriosus: an autosomal recessive disease?].
    le Marec B; Odent S; Almange C; Journel H; Roussey M; Defawe G
    J Genet Hum; 1989 Sep; 37(3):225-30. PubMed ID: 2625625
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.
    Froster UG; Rehder H; Höhn W; Oberheuser F
    Am J Med Genet; 1993 Oct; 47(5):717-22. PubMed ID: 8267003
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Consanguinity and the transmission/disequilibrium test for allelic association.
    Bennett S; Curnow RN
    Genet Epidemiol; 2001 Jul; 21(1):68-77. PubMed ID: 11443735
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal-recessive inheritance of benign recurrent intrahepatic cholestasis.
    De Koning TJ; Sandkuijl LA; De Schryver JE; Hennekam EA; Beemer FA; Houwen RH
    Am J Med Genet; 1995 Jul; 57(3):479-82. PubMed ID: 7677155
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Unilateral isolated microphthalmia inherited as an autosomal recessive trait.
    Fleckenstein M; Maumenee IH
    Ophthalmic Genet; 2005 Dec; 26(4):163-8. PubMed ID: 16352476
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Additional case of opsismodysplasia supporting autosomal recessive inheritance.
    Beemer FA; Kozlowski KS
    Am J Med Genet; 1994 Feb; 49(3):344-7. PubMed ID: 8209898
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies: a new autosomal recessive syndrome?
    Kotzot D; Richter K; Gierth-Fiebig K
    Am J Med Genet; 1994 Apr; 50(3):224-7. PubMed ID: 8042664
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new category of lethal short-limbed dwarfism.
    Knowles S; Winter R; Rimoin D
    Am J Med Genet; 1986 Sep; 25(1):41-6. PubMed ID: 3799722
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Brazilian family with quadrupedal gait, severe mental retardation, coarse facial characteristics, and hirsutism.
    Garcias Gde L; Roth Mda G
    Int J Neurosci; 2007 Jul; 117(7):927-33. PubMed ID: 17613106
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.