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 *

112 related articles for article (PubMed ID: 1601482)

  • 1. Renal glycosuria in two siblings.
    Havaldar PV; Mahantshetty NS; Siddibhavi BM
    Indian Pediatr; 1992 Jan; 29(1):114-6. PubMed ID: 1601482
    [No Abstract]   [Full Text] [Related]  

  • 2. [Renal glycosuria: dominant or recessive autosome anomaly? Mode of hereditary transmission based on the analysis of a 3-generation family tree].
    De Marchi S; Proto G; Jengo A; Collinassi P; Basile A
    Minerva Med; 1983 Feb; 74(7):301-6. PubMed ID: 6828258
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Glucose reabsorption in familial renal glycosuria and glucose-galactose malabsorption.
    Elsas LJ
    Birth Defects Orig Artic Ser; 1970 Sep; 6(3):21-2. PubMed ID: 5522782
    [No Abstract]   [Full Text] [Related]  

  • 4. Renal glycosuria (a family study).
    Dash R; Mishra K; Das PC; Das RK; Mohakur AC; Padhi PK; Mishra D
    J Indian Med Assoc; 1984 Aug; 82(8):287-9. PubMed ID: 6491338
    [No Abstract]   [Full Text] [Related]  

  • 5. [Morphological and cytogenetic correlations in some congenital malformations].
    Chipail A; Constantinescu V; Haimovici M; Scripcaru G; Harmanschi A
    Rev Med Chir Soc Med Nat Iasi; 1969; 73(1):27-34. PubMed ID: 4240580
    [No Abstract]   [Full Text] [Related]  

  • 6. Congenital factor XIII deficiency.
    Shukla J; Dube B; Dube RK; Das BK; Mishra OP
    J Assoc Physicians India; 1993 Nov; 41(11):731. PubMed ID: 8005932
    [No 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. MCAD deficiency in the Holderman Mennonite population in central Kansas.
    Casey JL
    Kans Med; 1992 Nov; 93(11):306-8. PubMed ID: 1460814
    [No Abstract]   [Full Text] [Related]  

  • 9. Progressive bulbar palsy of childhood in siblings.
    Benjamins D
    Ann Neurol; 1980 Aug; 8(2):203. PubMed ID: 7425580
    [No Abstract]   [Full Text] [Related]  

  • 10. Novel splice site mutation of aspartoacylase gene in a Turkish patient with Canavan disease.
    Rady PL; Penzien JM; Vargas T; Tyring SK; Matalon R
    Eur J Paediatr Neurol; 2000; 4(1):27-30. PubMed ID: 10701101
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2).
    van den Heuvel LP; Assink K; Willemsen M; Monnens L
    Hum Genet; 2002 Dec; 111(6):544-7. PubMed ID: 12436245
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The spinocerebellar ataxias: molecular progress and newly recognized paediatric phenotypes.
    Morrison PJ
    Eur J Paediatr Neurol; 2000; 4(1):9-15. PubMed ID: 10701099
    [No Abstract]   [Full Text] [Related]  

  • 13. [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]  

  • 14. [Bilateral anophthalmus--a rare autosomal recessive disease picture].
    Konopizky BE; Endres M
    Fortschr Ophthalmol; 1984; 81(4):383-4. PubMed ID: 6479810
    [No Abstract]   [Full Text] [Related]  

  • 15. Aminopterin Syndrome Sine Aminopterin (ASSA) syndrome in two siblings: further delineation of the syndrome and review of the literature.
    Krajewska-Walasek M
    Genet Couns; 1994; 5(4):345-55. PubMed ID: 7888136
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A syndrome of mental retardation, short stature, craniofacial anomalies with palpebral ptosis and pulmonary stenosis in three siblings with normal parents. An example of autosomal recessive inheritance of the Noonan phenotype?
    Maximilian C; Ioan DM; Fryns JP
    Genet Couns; 1992; 3(2):115-8. PubMed ID: 1642809
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ataxia telangiectasia.
    Paruthi SC; Singh H; Singh H
    J Assoc Physicians India; 1991 Feb; 39(2):215-6. PubMed ID: 1885492
    [No Abstract]   [Full Text] [Related]  

  • 18. Language and learning skill of hearing-impaired students. Genetic evaluation.
    Smith S; Kimberling WJ
    ASHA Monogr; 1986 Mar; (23):9-11. PubMed ID: 3730037
    [No Abstract]   [Full Text] [Related]  

  • 19. [Congenital autosomal-recessive familial spastic paraplegia].
    Badalian LO; Umakhanov RU; Temin PA; Arhipov BA; Bulaeva NV; Sakidebirov GM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(8):97-9. PubMed ID: 1661531
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Meckel-Gruber syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Jan; 14(1):32-5. PubMed ID: 8451225
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.