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 *

277 related articles for article (PubMed ID: 8741931)

  • 1. Autosomal dominant Russell-Silver syndrome.
    Al-Fifi S; Teebi AS; Shevell M
    Am J Med Genet; 1996 Jan; 61(1):96-7. PubMed ID: 8741931
    [No Abstract]   [Full Text] [Related]  

  • 2. New syndrome: familial proportionate short stature, intrauterine growth retardation, and recurrent locking of the fingers.
    Eng CE; Strom CM
    Am J Med Genet; 1987 Jan; 26(1):217-20. PubMed ID: 3812565
    [No Abstract]   [Full Text] [Related]  

  • 3. Partial trisomy 17p12pter, associated with pre and postnatal growth retardation, dysmorphic facial and digital features, developmental delay, and signs of HMSN1 in early childhood.
    Vogt J; Hill S; Brueton L
    Eur J Med Genet; 2006; 49(5):439-43. PubMed ID: 16488202
    [No Abstract]   [Full Text] [Related]  

  • 4. The Dubowitz syndrome.
    Wilroy RS; Tipton RE; Summitt RL
    Am J Med Genet; 1978; 2(3):275-84. PubMed ID: 263660
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Three-generation dominant transmission of the Silver-Russell syndrome.
    Duncan PA; Hall JG; Shapiro LR; Vibert BK
    Am J Med Genet; 1990 Feb; 35(2):245-50. PubMed ID: 2178417
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Silver-Russell syndrome and its genetic origins.
    Rossignol S
    J Endocrinol Invest; 2006; 29(1 Suppl):9-10. PubMed ID: 16615300
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Monozygotic twins discordant for the Russell-Silver syndrome.
    Samn M; Lewis K; Blumberg B
    Am J Med Genet; 1990 Dec; 37(4):543-5. PubMed ID: 2260605
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Child with Sotos phenotype and a 5:15 translocation.
    Maroun C; Schmerler S; Hutcheon RG
    Am J Med Genet; 1994 Apr; 50(3):291-3. PubMed ID: 8042674
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation.
    Morillo-Cucci G; Passarge E; Simpson JL; Chaganti RS; German J
    Birth Defects Orig Artic Ser; 1975; 11(2):380-3. PubMed ID: 1227554
    [No Abstract]   [Full Text] [Related]  

  • 10. [Russell-Silver syndrome].
    Kosaki K; Izumi K; Hasegawa T
    Nihon Rinsho; 2006 Sep; Suppl 3():436-9. PubMed ID: 17022582
    [No Abstract]   [Full Text] [Related]  

  • 11. 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]  

  • 12. Pitt-Rogers-Danks syndrome: further delineation.
    Lizcano-Gil LA; García-Cruz D; García-Cruz O; Sánchez-Corona J
    Am J Med Genet; 1995 Feb; 55(4):420-2. PubMed ID: 7762580
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ruvalcaba syndrome: autosomal dominant inheritance.
    Sugio Y; Kajii T
    Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An autosomal dominant syndrome of characteristic facial appearance, preauricular pits, fifth finger clinodactyly, and tetralogy of Fallot.
    Jones MC; Waldman JD
    Am J Med Genet; 1985 Sep; 22(1):135-41. PubMed ID: 4050848
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Silver-Russell syndrome. Presentation of a case with autosomal dominant heredity].
    Zanchetta S; Praderio R; Marcer G; Bagnani A
    Pediatr Med Chir; 1990; 12(3):277-9. PubMed ID: 2274440
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Growth deficiency, facial dysmorphogenesis and brachydactyly: a new syndrome.
    Frias JL; Guttery EG; Felman AH
    Birth Defects Orig Artic Ser; 1975; 11(2):30-3. PubMed ID: 1227535
    [No Abstract]   [Full Text] [Related]  

  • 17. Clinical and molecular findings in two patients with russell-silver syndrome and UPD7: comparison with non-UPD7 cases.
    Bernard LE; Peñaherrera MS; Van Allen MI; Wang MS; Yong SL; Gareis F; Langlois S; Robinson WP
    Am J Med Genet; 1999 Nov; 87(3):230-6. PubMed ID: 10564876
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of two new polymorphisms (c2447-125A>G; c2532G>A) in the gamma 2-COP (COPG2) gene by screening of Silver-Russell syndrome patients.
    Mergenthaler S; Blagitko-Dorfs N; Wollmann HA; Ranke MB; Ropers HH; Kalscheuer VM; Eggermann T
    Hum Mutat; 2000 Jul; 16(1):96. PubMed ID: 10874328
    [No Abstract]   [Full Text] [Related]  

  • 19. Conductive deafness, symphalangism, and facial abnormalities: the WL syndrome in a Japanese family.
    Higashi K; Inoue S
    Am J Med Genet; 1983 Sep; 16(1):105-9. PubMed ID: 6638061
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bilateral branchial cleft sinuses associated with intrauterine and postnatal growth retardation, premature aging, and unusual facial appearance: a new syndrome with dominant transmission.
    Lee WK; Root AW; Fenske N
    Am J Med Genet; 1982 Mar; 11(3):345-52. PubMed ID: 7200726
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.