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 *

87 related articles for article (PubMed ID: 9489787)

  • 1. Prenatal growth retardation, pelvic hypoplasia, and arthrogrypotic changes of lower limbs: a distinct autosomal-recessive disorder.
    Sarralde A; Reynoso MC; Nazará Z; Soto F; Hernández A
    Am J Med Genet; 1998 Feb; 75(5):453-60. PubMed ID: 9489787
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder.
    Cantú JM; Rivera H; Nazará Z; Rojas Q; Hernández A; García-Cruz D
    Clin Genet; 1980 Sep; 18(3):153-9. PubMed ID: 7192193
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome.
    Schrander-Stumpel C; de Die-Smulders C; Fryns JP; da Costa J; Bouckaert P
    Am J Med Genet; 1990 Sep; 37(1):133-5. PubMed ID: 2240030
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial distal arthrogryposis type I.
    Stoll C; Alembik Y; Dott B
    Ann Genet; 1996; 39(2):75-80. PubMed ID: 8766137
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Limb-pelvis hypoplasia/aplasia: a discrete entity in the fibuloulnar developmental field complex.
    Genuardi M; Gasparini P; Neri G; Zelante L
    Am J Med Genet; 1997 Jan; 68(2):190-4. PubMed ID: 9028457
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A fatal autosomal recessive syndrome with multiple congenital contractures].
    Herva R; Leisti J; Kirkinen P; Seppänen U; Martikainen J
    Duodecim; 1985; 101(8):756-62. PubMed ID: 4039655
    [No Abstract]   [Full Text] [Related]  

  • 7. Familial aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits in an inbred Pakistani Muslim family: a possible new autosomal recessive disorder with overlapping manifestations of the syndromes of Fuhrmann, Al-Awadi, and Raas-Rothschild.
    Kumar D; Duggan MB; Mueller RF; Karbani G
    Am J Med Genet; 1997 May; 70(2):107-13. PubMed ID: 9128926
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pelvic dysplasia associated with arthrogrypotic changes in the lower extremities. A new syndrome.
    Ray S; Peterson PD; Scott CI
    Clin Orthop Relat Res; 1986 Jun; (207):99-102. PubMed ID: 3720110
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Part I. Amyoplasia: a common, sporadic condition with congenital contractures.
    Hall JG; Reed SD; Driscoll EP
    Am J Med Genet; 1983 Aug; 15(4):571-90. PubMed ID: 6614047
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Adams-Oliver syndrome: further evidence of an autosomal recessive variant.
    Temtamy SA; Aglan MS; Ashour AM; Zaki MS
    Clin Dysmorphol; 2007 Jul; 16(3):141-149. PubMed ID: 17551326
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Characterization of a group unrelated patients with arthrogryposis multiplex congenita.
    Valdés-Flores M; Casas-Avila L; Hernández-Zamora E; Kofman S; Hidalgo-Bravo A
    J Pediatr (Rio J); 2016; 92(1):58-64. PubMed ID: 26453511
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cortical blindness, growth and psychomotor retardation and postaxial polydactyly: a probably distinct autosomal recessive syndrome.
    Hernández A; García-Esquivel L; Reynoso MC; Fragoso R; Enríquez-Guerra MA; Nazará Z; Anzar MB; Cantú JM
    Clin Genet; 1985 Sep; 28(3):251-4. PubMed ID: 4064363
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Limb/pelvis-hypoplasia/aplasia syndrome--further delineation of phenotype.
    Gupta N; Kabra M
    Fetal Pediatr Pathol; 2011; 30(6):355-8. PubMed ID: 21895521
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autosomal dominant B-cell immunodeficiency, distal limb anomalies and urogenital malformations (BILU syndrome) - report of a second family.
    Tischkowitz M; Goodman F; Koliou M; Webster D; Edery P; Jones A; Wilson LC
    Clin Genet; 2004 Dec; 66(6):550-5. PubMed ID: 15521984
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Neu-Laxova syndrome in female sibs: clinical and pathological features with prenatal diagnosis in the second sib.
    Tolmie JL; Mortimer G; Doyle D; McKenzie R; McLaurin J; Neilson JP
    Am J Med Genet; 1987 May; 27(1):175-82. PubMed ID: 3300330
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New hereditary malformation syndrome of unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defects.
    Middleton LT; Anastasiades V; Panayidou K; Georghiou D; Kalli E; Gabriel G; Myrianthopoulos NC
    Am J Med Genet; 1992 Dec; 44(6):757-61. PubMed ID: 1481843
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Report of a rare distal arthrogrophy large family].
    Jiang M; Han WT; Bian CY; Wang G; Li WZ; Sun LN; Yang Z
    Yi Chuan; 2004 Nov; 26(6):803-6. PubMed ID: 15640106
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Metaphyseal anadysplasia in two sisters.
    Slama M; Mathieu M; Dehouck I; al Hosri J; Vanthournout I; Baratte B; Grumbach Y
    Pediatr Radiol; 1999 May; 29(5):372-5. PubMed ID: 10382218
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Syndrome of mental retardation, facial anomalies, hypopituitarism, and distal arthrogryposis in sibs.
    Chitayat D; Hall JG; Couch RM; Phang MS; Baldwin VJ
    Am J Med Genet; 1990 Sep; 37(1):65-70. PubMed ID: 2240046
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Polysyndactylia with brachymetacarpia (Type Bonola)].
    Kunze J; Lenz W; Sugiura Y; Yang TS
    Klin Padiatr; 1992; 204(1):43-7. PubMed ID: 1311046
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.