BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 1381884)

  • 1. Ring chromosome 17. Case report and review of the literature.
    Teyssier M; Charrin C; Corgiolu Theuil G; David L
    Ann Genet; 1992; 35(2):75-8. PubMed ID: 1381884
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies.
    Melnyk AR; Dewald G
    Am J Med Genet; 1994 Mar; 50(1):12-4. PubMed ID: 7512788
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Ring chromosome 21 as a cause of developmental disorder. A case report from the practice of child psychiatry].
    Melkild A
    Tidsskr Nor Laegeforen; 1994 Jan; 114(1):36-8. PubMed ID: 7507604
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ring chromosome 8 associated with microcephaly.
    Mingarelli R; Valorani G; Zelante L; Dallapiccola B
    Ann Genet; 1991; 34(2):90-2. PubMed ID: 1746890
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A study of ring 20 chromosome karyotype with epilepsy.
    Yamadera H; Kobayashi K; Sugai K; Suda H; Kaneko S
    Psychiatry Clin Neurosci; 1998 Feb; 52(1):63-8. PubMed ID: 9682935
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial inverted duplication 7p.
    Schaefer GB; Novak K; Steele D; Buehler B; Smith S; Zaleski D; Pickering D; Nelson M; Sanger W
    Am J Med Genet; 1995 Mar; 56(2):184-7. PubMed ID: 7542835
    [TBL] [Abstract][Full Text] [Related]  

  • 7. "Ring syndrome" involving chromosome 2 confirmed by FISH analysis using chromosome-specific subtelomeric probes.
    Kosho T; Matsushima K; Sahashi T; Mitsui N; Fukushima Y; Sobajima H; Ohashi H
    Genet Couns; 2005; 16(1):65-70. PubMed ID: 15844781
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Familial Miller-Dieker syndrome and (15;17) chromosome translocation].
    Goutières F; Aicardi J; Rethore MO; Prieur M; Lejeune J
    Arch Fr Pediatr; 1987; 44(7):501-4. PubMed ID: 3426372
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ring chromosome 15 syndrome in an adult female.
    Matsuishi T; Yamada Y; Endo K; Sakai H; Fukushima Y
    J Intellect Disabil Res; 1996 Oct; 40 ( Pt 5)():478-80. PubMed ID: 8906535
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome.
    Ricard-Mousnier B; N'Guyen S; Dubas F; Pouplard F; Guichet A
    Epileptic Disord; 2007 Sep; 9(3):327-31. PubMed ID: 17884758
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Developmental delay, short stature, and minor facial anomalies in a child with ring chromosome 16.
    Chodirker BN; Ray M; McAlpine PJ; Riordan D; Vust A; Pugh D; Chudley AE
    Am J Med Genet; 1988 Sep; 31(1):145-51. PubMed ID: 2464927
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Brief clinical report: interstitial deletion of the long arm of chromosome 10: del(10)(q11.2q21).
    Holden JJ; MacDonald EA
    Am J Med Genet; 1985 Feb; 20(2):245-8. PubMed ID: 2579554
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A case of the ring 20 syndrome.
    Thomsen SG; Petersen MB; Andersen EA; ostergaard GZ; Lindenberg S
    Ann Genet; 1989; 32(2):111-3. PubMed ID: 2757359
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Meiotic origin of two ring chromosomes 18 in a girl with developmental delay.
    Baumer A; Giovannucci Uzielli ML; Guarducci S; Lapi E; Röthlisberger B; Schinzel A
    Am J Med Genet; 2002 Nov; 113(1):101-4. PubMed ID: 12400074
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ring chromosome 5 associated with severe growth retardation as the sole major physical abnormality.
    Migliori MV; Cherubini V; Bartolotta E; Pettinari A; Pecora R
    Am J Med Genet; 1994 Jan; 49(1):108-10. PubMed ID: 8172236
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Small terminal deletions of the long arm of chromosome 2: two new cases.
    Fisher AM; Ellis KH; Browne CE; Barber JC; Barker M; Kennedy CR; Foley H; Patton MA
    Am J Med Genet; 1994 Dec; 53(4):366-9. PubMed ID: 7532357
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Terminal deletion of long arm of chromosome 4: patient report and literature review.
    Evers LJ; Schrander-Stumpel CT; Engelen JJ; Mulder H; Borghgraef M; Fryns JP
    Genet Couns; 1993; 4(2):139-45. PubMed ID: 7689326
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ring chromosome 15 involving deletion of the insulin-like growth factor 1 receptor gene in a patient with features of Silver-Russell syndrome.
    Tamura T; Tohma T; Ohta T; Soejima H; Harada N; Abe K; Niikawa N
    Clin Dysmorphol; 1993 Apr; 2(2):106-13. PubMed ID: 7506614
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.
    Battaglia A; Hoyme HE; Dallapiccola B; Zackai E; Hudgins L; McDonald-McGinn D; Bahi-Buisson N; Romano C; Williams CA; Brailey LL; Zuberi SM; Carey JC
    Pediatrics; 2008 Feb; 121(2):404-10. PubMed ID: 18245432
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deletion (9) (p13.1 p21.1).
    Scaglia F; Bodamer OA; Berend SA; Adam LR; Shaffer LG
    Am J Med Genet; 2000 Mar; 91(2):113-5. PubMed ID: 10748408
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.