BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 2581446)

  • 21. Autosomal recessive Silver-Russell syndrome.
    Teebi AS
    Clin Dysmorphol; 1992 Jul; 1(3):151-6. PubMed ID: 1285272
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ocular manifestations of Sotos syndrome.
    Maino DM; Kofman J; Flynn MF; Lai L
    J Am Optom Assoc; 1994 May; 65(5):339-46. PubMed ID: 8071505
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Multiple giant pilomatricoma in familial Sotos syndrome.
    Gilaberte Y; Ferrer-Lozano M; Oliván MJ; Coscojuela C; Abascal M; Lapunzina P
    Pediatr Dermatol; 2008; 25(1):122-5. PubMed ID: 18304174
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism.
    Faivre L; Viot G; Prieur M; Turleau C; Gosset P; Romana S; Munnich A; Vekemans M; Cormier-Daire V
    Am J Med Genet; 2000 Apr; 91(4):273-6. PubMed ID: 10766982
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Craniofacial pattern profile (CFPP) evaluation of facial dysmorphology in a familial syndrome with corneal anesthesia and multiple congenital anomalies.
    Saksena SS; Ramos-Arroyo MA; Hodes ME
    Am J Phys Anthropol; 1987 Dec; 74(4):465-71. PubMed ID: 3442298
    [TBL] [Abstract][Full Text] [Related]  

  • 26. SHORT syndrome: a new case with probable autosomal dominant inheritance.
    Sorge G; Ruggieri M; Polizzi A; Scuderi A; Di Pietro M
    Am J Med Genet; 1996 Jan; 61(2):178-81. PubMed ID: 8669449
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Maxillonasal dysplasia (Binder's syndrome). A study of craniofacial morphology, associated malformations and familial relations.
    Olow-Nordenram M
    Swed Dent J Suppl; 1987; 47():1-38. PubMed ID: 3499673
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Like father, like son: periventricular nodular heterotopia and nonverbal learning disorder.
    McCann MV; Pongonis SJ; Golomb MR; Edwards-Brown M; Christensen CK; Sokol DK
    J Child Neurol; 2008 Aug; 23(8):950-3. PubMed ID: 18660478
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Psychosocial, cognitive, and motor functioning in patients with suspected Sotos syndrome: a comparison between patients with and without NSD1 gene alterations.
    de Boer L; Röder I; Wit JM
    Dev Med Child Neurol; 2006 Jul; 48(7):582-8. PubMed ID: 16780628
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Investigations in dominant Sotos syndrome.
    Smith A; Farrar JR; Silink M; Judzewitsch R
    Ann Genet; 1981; 24(4):226-8. PubMed ID: 6977303
    [No Abstract]   [Full Text] [Related]  

  • 31. [Cerebral gigantism--Sotos' syndrome].
    Eskeland P
    Tidsskr Nor Laegeforen; 1990 Feb; 110(5):600-1. PubMed ID: 2309210
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Soto's syndrome (cerebral gigantism)].
    Jović NS; Vranjesević DN; Jović JZ; Marinković DD
    Srp Arh Celok Lek; 1996; 124(1-2):37-40. PubMed ID: 9102812
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Sotos syndrome: evolution of facial phenotype subjective and objective assessment.
    Allanson JE; Cole TR
    Am J Med Genet; 1996 Oct; 65(1):13-20. PubMed ID: 8914735
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A new syndrome with distinct facial and auricular malformations and dominant inheritance.
    Simosa V; Penchaszadeh VB; Bustos T
    Am J Med Genet; 1989 Feb; 32(2):184-6. PubMed ID: 2929657
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Chronic renal failure in a patient with Sotos syndrome due to autosomal dominant polycystic kidney disease.
    Cefle K; Yildiz A; Palanduz S; Ozturk S; Ozbey N; Kylyçaslan I; Colakoglu S; Balci C
    Int J Clin Pract; 2002 May; 56(4):316-8. PubMed ID: 12074220
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Dysmorphic growth and development and the study of craniofacial syndromes.
    Cohen MM
    J Craniofac Genet Dev Biol Suppl; 1985; 1():43-55. PubMed ID: 3877108
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Metacarpophalangeal pattern profile analysis in 14 Japanese children with Sotos syndrome.
    Takahashi Y; Imaizumi K; Takada F; Kuroki Y
    Jpn J Hum Genet; 1994 Mar; 39(1):187-91. PubMed ID: 8025295
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Craniofacial and dental characteristics of Silver-Russell syndrome.
    Kotilainen J; Hölttä P; Mikkonen T; Arte S; Sipilä I; Pirinen S
    Am J Med Genet; 1995 Mar; 56(2):229-36. PubMed ID: 7625451
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndrome.
    Tong TM; Hau EW; Lo IF; Chan DH; Lam ST
    Chin Med J (Engl); 2005 Sep; 118(18):1499-506. PubMed ID: 16232326
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Coffin-Lowry syndrome. Description of a clinical case].
    Venura A; Ferrari P; Benci E; Grando A
    Pediatr Med Chir; 1988; 10(4):449-50. PubMed ID: 3231552
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.