BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 8330452)

  • 41. Mental retardation, distinct craniofacial dysmorphism, and central nervous system malformation: confirmation of a syndrome.
    Devriendt K; D'Espallier L; Fryns JP
    J Med Genet; 1996 Mar; 33(3):224-6. PubMed ID: 8728696
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Duplication of the short arm of the X chromosome in mother and daughter.
    Tuck-Muller CM; Martinez JE; Batista DA; Kearns WG; Wertelecki W
    Hum Genet; 1993 May; 91(4):395-400. PubMed ID: 8500796
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A 48, XXXX female.
    Peña SD; Ray M; Douglas G; Loadman E; Hamerton JL
    J Med Genet; 1974 Jun; 11(2):211-5. PubMed ID: 4842278
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A de novo complex chromosomal rearrangement with nine breakpoints characterized by FISH in a boy with mild mental retardation, developmental delay, short stature and microcephaly.
    Joyce CA; Cabral de Almeida JC; Santa Rose AA; Correia P; Moraes L; Bastos E; Llerena J
    Clin Genet; 1999 Jul; 56(1):86-92. PubMed ID: 10466423
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Twenty-six years later: a woman with tetra-X chromosomes.
    Berg JM; Karlinsky H; Korossy M; Pakula Z
    J Ment Defic Res; 1988 Feb; 32 ( Pt 1)():67-74. PubMed ID: 3361607
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Fragile X syndrome: a major cause of X-linked mental retardation.
    Butler MG
    Compr Ther; 1988 Jul; 14(7):3-7. PubMed ID: 3060303
    [No Abstract]   [Full Text] [Related]  

  • 47. Apparent homozygosity for the fragile site at Xq28 in a normal female.
    Nielsen KB; Tommerup N; Poulsen H; Mikkelsen M
    Hum Genet; 1982; 61(1):60-2. PubMed ID: 7129428
    [No Abstract]   [Full Text] [Related]  

  • 48. Radioulnar synostosis, behavioral disturbance, and XYY chromosomes.
    Cleveland WW; Arias D; Smith GF
    J Pediatr; 1969 Jan; 74(1):103-6. PubMed ID: 5782813
    [No Abstract]   [Full Text] [Related]  

  • 49. Marker X chromosomes in nonspecific male mental retardation.
    Venter PA; Gericke GS
    S Afr Med J; 1980 Jun; 57(26):1066. PubMed ID: 7190736
    [No Abstract]   [Full Text] [Related]  

  • 50. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L; Corsello G; Giuffrè M; Piccione M; Albanese A
    Am J Med Genet; 1994 Jul; 51(3):266-9. PubMed ID: 8074157
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Clinical delineation of Giuffrè-Tsukahara syndrome: another case with microcephaly and radio-ulnar synostosis with apparent X-linked semi-dominant inheritance.
    Gaspar H; Albermann K; Baumer A; Schinzel A
    Am J Med Genet A; 2008 Jun; 146A(11):1453-7. PubMed ID: 18449925
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Cardio-facio cutaneous syndrome: neurological manifestations.
    Gross-Tsur V; Gross-Kieselstein E; Amir N
    Clin Genet; 1990 Nov; 38(5):382-6. PubMed ID: 2149308
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Endocrine function and diagnostic problems in a prepubertal case of 48,XXYY.
    Vigi V; Pinca A; Guerrini P; Scappaticci S; Volpato S
    J Genet Hum; 1978 Dec; 26(4):411-7. PubMed ID: 571897
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Additional case of Tsukahara's syndrome or new syndrome: further delineation of the association of microcephaly and radio-ulnar synostosis.
    Selicorni A; Ferrarini A; Cagnoli G; Fratoni A; Bottigelli M; Milani D
    Am J Med Genet A; 2005 Jan; 132A(2):189-90. PubMed ID: 15578583
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Penta-X syndrome. Report of a case with 47,XXX/48,XXXX/49,XXXXX mosaicism].
    Gómez-Valencia L; Nájera-Martínez P; Morales-Hernández A; Martínez-Díaz De León A
    Bol Med Hosp Infant Mex; 1989 Jun; 46(6):417-21. PubMed ID: 2665783
    [TBL] [Abstract][Full Text] [Related]  

  • 56. FG syndrome: the trias mental retardation, hypotonia and constipation reviewed.
    Zwamborn-Hanssen AM; Schrander-Stumpel CT; Smeets E; Decock P; Fryns JP
    Genet Couns; 1995; 6(4):313-9. PubMed ID: 8775418
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Three cases of sex chromosome mosaicism with a nonfluorescent Y.
    Madan K; Gooren L; Schoemaker J
    Hum Genet; 1979 Feb; 46(3):295-304. PubMed ID: 437772
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Combined deletion 18q22.2 and duplication/triplication 18q22.1 causes microcephaly, mental retardation and leukencephalopathy.
    Nguyen-Minh S; Drossel K; Horn D; Rost I; Spors B; Kaindl AM
    Gene; 2013 Jul; 523(1):92-8. PubMed ID: 23566840
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A 49,XXXYY male.
    Salamanca-Gòmez F; Cortès R; Sànchez J; Armendares S
    Am J Med Genet; 1981; 10(4):351-5. PubMed ID: 7199254
    [No Abstract]   [Full Text] [Related]  

  • 60. Neurodevelopmental and psychological aspects in a child with 49XYYYY karyotype.
    Sirota L; Shaghapour SE; Elitzur A; Sirota P
    Clin Genet; 1986 Dec; 30(6):471-4. PubMed ID: 3815880
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.