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 *

80 related articles for article (PubMed ID: 9580072)

  • 1. [Introduction to molecular biology and its application to pediatrics (8): additional methods for the detection of mutations. Clinical case: hemochromatosis in a family. Transgenic animals].
    Castaño L; Bilbao JR; Pérez de Nanclares G
    An Esp Pediatr; 1997 Dec; 47(6):653-8. PubMed ID: 9580072
    [No Abstract]   [Full Text] [Related]  

  • 2. [Introduction to molecular biology and its application to pediatrics (5): clinical cases. Genetic alterations in XY gonadal dysgenesis and in myotonic dystrophy].
    Castaño L; Bilbao JR; Urrutia I
    An Esp Pediatr; 1997 May; 46(5):513-8. PubMed ID: 9297412
    [No Abstract]   [Full Text] [Related]  

  • 3. [Family screening strategy for genetic hemochromatosis].
    Deugnier Y; Fauchet R; Brissot P
    Gastroenterol Clin Biol; 1990; 14(8-9):662-8. PubMed ID: 2227239
    [No Abstract]   [Full Text] [Related]  

  • 4. [A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis].
    Andrikovics H; Klein I; Kalmár L; Bors A; Jermendy G; Petri I; Kalász L; Váradi A; Tordai A
    Orv Hetil; 1999 Nov; 140(45):2517-22. PubMed ID: 10586619
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The contribution of molecular genetics to the nosology and diagnosis of neurological disorders of childhood].
    Aicardi J
    Rev Neurol; 1999 Jan 1-15; 28(1):1-4. PubMed ID: 10101756
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Introduction to molecular biology and its application to pediatrics (7): concepts of genetics in hereditary diseases. Genetic banks].
    Castaño L; Bilbao JR
    An Esp Pediatr; 1997 Oct; 47(4):437-42. PubMed ID: 9499320
    [No Abstract]   [Full Text] [Related]  

  • 7. [Genetic molecular basis of epilepsy].
    Serratosa JM
    Rev Neurol; 1995; 23(124):1290-1. PubMed ID: 8556635
    [No Abstract]   [Full Text] [Related]  

  • 8. [Introduction to molecular biology and its application to pediatrics (6): clinical case: molecular disorder in central diabetes insipidus. Analysis of polymorphic gene: HLA type].
    Castaño L; Bilbao JR; Calvo B
    An Esp Pediatr; 1997 Aug; 47(2):201-6. PubMed ID: 9382358
    [No Abstract]   [Full Text] [Related]  

  • 9. [The introduction to molecular biology and its application go pediatrics (4): study of mutations in DNA amplified by PCR].
    Castaño L; Bilbao JR
    An Esp Pediatr; 1997 Mar; 46(3):305-10. PubMed ID: 9173859
    [No Abstract]   [Full Text] [Related]  

  • 10. Molecular genetics: what is it and what is its impact on current and future medical practice?
    Evans HJ
    Health Bull (Edinb); 1986 Nov; 44(6):319-29. PubMed ID: 3546195
    [No Abstract]   [Full Text] [Related]  

  • 11. [Introduction to molecular biology and its application to pediatrics (3): restriction enzymes. Polymerase chain reaction. Ways to study mutations].
    Castaño L; Bilbao JR; Calvo B
    An Esp Pediatr; 1997 Jan; 46(1):87-92. PubMed ID: 9082901
    [No Abstract]   [Full Text] [Related]  

  • 12. A rare case of a patient heterozygous for the hemochromatosis mutation C282Y and homozygous for H63D.
    Lucotte G; Champenois T; Sémonin O
    Blood Cells Mol Dis; 2001; 27(5):892-3. PubMed ID: 11783952
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Diagnostic strategies in inherited hemochromatosis. Value of the genetic test].
    Fábrega García E; Pons Romero F
    Rev Clin Esp; 2000 Sep; 200(9):516-9. PubMed ID: 11111398
    [No Abstract]   [Full Text] [Related]  

  • 14. [Value of genetic diagnosis of C282Y mutation in patients with hereditary hemochromatosis].
    Ocran K; Schmidt HH
    Z Gastroenterol; 2000 Feb; 38(2):205-7. PubMed ID: 10721178
    [No Abstract]   [Full Text] [Related]  

  • 15. Molecular genetics of hereditary neuropathies.
    Chance PF
    J Child Neurol; 1999 Jan; 14(1):43-52. PubMed ID: 10223854
    [No Abstract]   [Full Text] [Related]  

  • 16. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
    Lee PL; Gelbart T; West C; Halloran C; Beutler E
    Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Study of the gene of hemochromatosis in first degree relatives of patient with porphyria cutanea tarda].
    García-Morillo JS; Carneado de la Fuente J; Stiefel García-Junco P; García-Donas MA; González Escribano MF; Núñez-Roldán A
    Med Clin (Barc); 1999 May; 112(18):699-701. PubMed ID: 10374203
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The involvement of myelin proteins in hereditary neuropathies].
    Sindou P; Anani T; Garbay B; Couratier P; Lagrange E; Vallat JM
    Rev Neurol (Paris); 1999 Feb; 155(2):97-110. PubMed ID: 10226313
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree.
    Richards JE; Ritch R; Lichter PR; Rozsa FW; Stringham HM; Caronia RM; Johnson D; Abundo GP; Willcockson J; Downs CA; Thompson DA; Musarella MA; Gupta N; Othman MI; Torrez DM; Herman SB; Wong DJ; Higashi M; Boehnke M
    Ophthalmology; 1998 Sep; 105(9):1698-707. PubMed ID: 9754180
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Gly380Arg and Asn540Lys mutations of fibroblast growth factor receptor 3 in achondroplasia and hypochndroplasia in the Spanish population].
    Ezquieta Zubicaray B; Iguacel AO; Varela Junquera JM; Jariego Fente CM; González Gancedo P; Gracia Bouthelier R
    Med Clin (Barc); 1999 Mar; 112(8):290-3. PubMed ID: 10207844
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.