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 *

176 related articles for article (PubMed ID: 466847)

  • 21. Molecular cytogenetic analysis of a familial pericentric inversion of chromosome 12.
    Speleman F; Van Roy N; De Vos E; Hilliker C; Suijkerbuijk RF; Leroy JG
    Clin Genet; 1993 Sep; 44(3):156-63. PubMed ID: 8275576
    [TBL] [Abstract][Full Text] [Related]  

  • 22. De novo direct duplication 2 (p12-->p21) with paternally inherited pericentric inversion 2p11.2 2q12.2.
    Magee AC; Humphreys MW; McKee S; Stewart M; Nevin NC
    Clin Genet; 1998 Jul; 54(1):65-9. PubMed ID: 9727743
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].
    Ayral D; Raudrant D; Charleux JP; Noel B
    Pediatrie; 1984 Dec; 39(8):681-90. PubMed ID: 6598632
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)].
    Wilson MG; Towner JW; Coffin GS; Ebbin AJ; Siris E; Brager P
    Hum Genet; 1981; 59(4):297-307. PubMed ID: 6949855
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Cri-du-chat syndrome and two other deformed children in a family carrying a pericentric inversion or insertion of chromosome 5].
    Delozier-Blanchet CD; Pitmon D; Schorderet D; Engel E
    J Genet Hum; 1985 Dec; 33(5):371-80. PubMed ID: 4093767
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Terminal deletion of the long arm of chromosome 4 in a mother and two sons.
    Descartes M; Keppler-Noreuil K; Knops J; Longshore JW; Finley WH; Carroll AJ
    Clin Genet; 1996 Dec; 50(6):538-40. PubMed ID: 9147894
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 'Complete 5p' trisomy: 1 case and 19 translocation carriers in 6 generations.
    Brimblecombe FS; Lewis FJ; Vowles M
    J Med Genet; 1977 Aug; 14(4):271-4. PubMed ID: 926139
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).
    van de Vooren MJ; Planteydt HT; Hagemeijer A; Peters-Slough MF; Timmerman MJ
    Clin Genet; 1984 Jan; 25(1):52-8. PubMed ID: 6705241
    [TBL] [Abstract][Full Text] [Related]  

  • 29. High resolution of a small pericentric inversion of chromosome 11.
    Autio-Harmainen H; De La Chapelle A
    J Med Genet; 1980 Feb; 17(1):44-7. PubMed ID: 7365763
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Interstitial deletion of the short arm of chromosome 4.
    Ray M; Evans J; Rockman-Greenberg C; Wickstrom D
    J Med Genet; 1984 Jun; 21(3):223-5. PubMed ID: 6748021
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Familial transmission of Wolf syndrome resulting from specific deletion 4p16 from t(4;8)(p16;p21) mat.
    Martsolf JT; Chase TR; Jalal SM; Wasdahl WA
    Clin Genet; 1987 Jun; 31(6):366-9. PubMed ID: 3621637
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Two unrelated children with distal long arm deletion of chromosome 7: clinical features, cytogenetic and gene marker studies.
    Bernstein R; Dawson B; Morcom G; Wagner J; Jenkins T
    Clin Genet; 1980; 17(3):228-37. PubMed ID: 6928813
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A girl with partial long-arm deletion of chromosome 11 and familial pericentric inversion of chromosome 9.
    Zabel B; Hansen S; Hilig U; Gröting-Imhof H
    Hum Genet; 1977 Apr; 36(1):117-22. PubMed ID: 858620
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Paracentric Inversion in man: personal experience and review of the literature.
    Fryns JP; Van den Berghe H
    Hum Genet; 1980; 54(3):413-6. PubMed ID: 7399530
    [No Abstract]   [Full Text] [Related]  

  • 35. Familial partial 7q monosomy resulting from segregation of an insertional chromosome rearrangement.
    Nielsen KB; Egede F; Mouridsen I; Mohr J
    J Med Genet; 1979 Dec; 16(6):461-6. PubMed ID: 537020
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Reproductive failure in a carrier of inv dupl l(q21.4----q12).
    Toncheva D; Genkova P; Tzoneva M; Lozanova T; Angelova E; Mitreva B
    Acta Paediatr Hung; 1986; 27(1):61-6. PubMed ID: 3730184
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Cat-like cry and mental retardation owing to 7q interstitial deletion (7q22 leads to 7q32).
    Abuelo DN; Padre-Mendoza T
    J Med Genet; 1982 Dec; 19(6):473-6. PubMed ID: 7154049
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Two cases with different deletions of the long arm of chromosome 7.
    Klep-de Pater JM; Bijlsma JB; Bleeker-Wagemakers EM; de France HF; de Vries-Ekkers CM
    J Med Genet; 1979 Apr; 16(2):151-4. PubMed ID: 458833
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Familial pericentric inversion (10) and its effect on two offspring.
    Rodriguez MT; Martin MJ; Abrisqueta JA
    J Med Genet; 1984 Aug; 21(4):317-9. PubMed ID: 6492099
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Familial transmission of a deletion of chromosome 21 derived from a translocation between chromosome 21 and an inverted chromosome 22.
    Aviv H; Lieber C; Yenamandra A; Desposito F
    Am J Med Genet; 1997 Jun; 70(4):399-403. PubMed ID: 9182781
    [TBL] [Abstract][Full Text] [Related]  

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