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 *

92 related articles for article (PubMed ID: 6072641)

  • 1. Persistent tachycardia, paroxymal hypertension, and seizures: association with hyperglycinuria, dominantly inherited microphthalmia, and cataracts.
    Adams CW; Nance WE
    JAMA; 1967 Nov; 202(6):525-30. PubMed ID: 6072641
    [No Abstract]   [Full Text] [Related]  

  • 2. Heritable Q-T prolongation without deafness.
    Garza LA; Vick RL; Nora JJ; McNamara DG
    Circulation; 1970 Jan; 41(1):39-48. PubMed ID: 5420631
    [No Abstract]   [Full Text] [Related]  

  • 3. Hyperglycinuria in a family with autosomal dominantly inherited cataract.
    Similä S; Käär ML
    Clin Genet; 1974; 6(2):138-41. PubMed ID: 4430153
    [No Abstract]   [Full Text] [Related]  

  • 4. Identification of PITX3 mutations in individuals with various ocular developmental defects.
    Zazo Seco C; Plaisancié J; Lupasco T; Michot C; Pechmeja J; Delanne J; Cottereau E; Ayuso C; Corton M; Calvas P; Ragge N; Chassaing N
    Ophthalmic Genet; 2018 Jun; 39(3):314-320. PubMed ID: 29405783
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial pancreatitis associated with hyperglycinuria.
    Bergström K; Hellström K; Kallner M; Lundh G
    Scand J Gastroenterol; 1973; 8(3):217-23. PubMed ID: 4724921
    [No Abstract]   [Full Text] [Related]  

  • 6. Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract.
    Miyamoto T; Yu YS; Sato H; Hayashi H; Sakugawa N; Ishikawa M; Sengoku K
    Turk J Pediatr; 2007; 49(3):334-6. PubMed ID: 17990594
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital cataract, microphthalmia and septal heart defect in two generations: a new syndrome?
    Wilkie AO; Taylor D; Scambler PJ; Baraitser M
    Clin Dysmorphol; 1993 Apr; 2(2):114-9. PubMed ID: 8281271
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inheritance of congenital cataracts and microphthalmia in the Miniature Schnauzer.
    Gelatt KN; Samuelson DA; Bauer JE; Das ND; Wolf ED; Barrie KP; Andresen TL
    Am J Vet Res; 1983 Jun; 44(6):1130-2. PubMed ID: 6870020
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic heterogeneity of the syndrome: microphthalmia with congenital cararact.
    Temtamy SA; Shalash BA
    Birth Defects Orig Artic Ser; 1974; 10(4):292-3. PubMed ID: 4470902
    [No Abstract]   [Full Text] [Related]  

  • 10. Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital cataracts.
    Bodker FS; Lavery MA; Mitchell TN; Lovrien EW; Maumenee IH
    Am J Med Genet; 1990 Sep; 37(1):54-9. PubMed ID: 2240043
    [TBL] [Abstract][Full Text] [Related]  

  • 11. HYPERGLYCINAEMIA AND HYPERGLYCINURIA IN A NEWBORN INFANT.
    VISSER HK; VEENSTRA HW; PIK C
    Arch Dis Child; 1964 Aug; 39(206):397-402. PubMed ID: 14206882
    [No Abstract]   [Full Text] [Related]  

  • 12. De novo inv(2)(p21q31) associated with isolated bilateral microphthalmia and cataracts.
    Weaver RG; Rao N; Thomas IT; Pettenati MJ
    Am J Med Genet; 1991 Sep; 40(4):509-12. PubMed ID: 1746620
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Idiopathic hyperglycinuria. III. Report of a second case.
    NYHAN WL; CHISOLM JJ; EDWARDS RO
    J Pediatr; 1963 Apr; 62():540-5. PubMed ID: 13939302
    [No Abstract]   [Full Text] [Related]  

  • 14. [Hyperglycinemia (glycinosis) with familial idiopathic hyperglycinuria. 1st observation in Germany].
    Diezel PB; Martin K
    Dtsch Med Wochenschr; 1966 Dec; 91(50):2249-54. PubMed ID: 5924250
    [No Abstract]   [Full Text] [Related]  

  • 15. Syndrome of microcephaly, microphthalmia, cataracts, and intracranial calcification.
    Slee J; Lam G; Walpole I
    Am J Med Genet; 1999 Jun; 84(4):330-3. PubMed ID: 10340646
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Glycine transport by cultured skin fibroblasts from a patient with isolated hyperglycinuria.
    Fénéant M; Moatti N; Lemonnier F; Maccario J; Gautier M; Charpentier C; Lemonnier A
    J Inherit Metab Dis; 1980; 3(3):97-8. PubMed ID: 6775149
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The inheritance of paroxysmal tachycardia.
    Ward OC
    G Ital Cardiol; 1972; 2(1):154. PubMed ID: 5011995
    [No Abstract]   [Full Text] [Related]  

  • 18. Familial atrial tachyarrhythmia with short PR interval.
    Brodsky M; Wu D; Denes P; Rosen KM
    Arch Intern Med; 1977 Feb; 137(2):165-9. PubMed ID: 836114
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spongy degeneration of the white matter of the central nervous system associated with hyperglycinuria.
    Rushton DI
    J Clin Pathol; 1968 Jul; 21(4):456-62. PubMed ID: 5748729
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2.
    Abouzeid H; Meire FM; Osman I; ElShakankiri N; Bolay S; Munier FL; Schorderet DF
    Ophthalmology; 2009 Jan; 116(1):154-162.e1. PubMed ID: 19004499
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.