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 *

96 related articles for article (PubMed ID: 6520016)

  • 21. Pitfalls in the use of chromosome variants for paternity dispute cases.
    Nakagome Y; Kitagawa T; Iinuma K; Matsunaga E; Shinoda T
    Hum Genet; 1977 Jul; 37(3):255-60. PubMed ID: 885544
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Three cases of 16q duplication.
    Maher ER; Willatt L; Cuthbert G; Chapman C; Hodgson SV
    J Med Genet; 1991 Nov; 28(11):801-2. PubMed ID: 1820771
    [No Abstract]   [Full Text] [Related]  

  • 23. Partial trisomy for 2q in a patient with dir dup(2) (q33.1q35).
    Romain DR; Mackenzie NG; Moss D; Columbano-Green LM; Smythe RH; Parfitt RG; Dixon JW
    J Med Genet; 1994 Aug; 31(8):652-3. PubMed ID: 7815427
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A case of partial monosomy 21q22.2 associated with Rieger's syndrome.
    Nielsen F; Trånebjaerg L
    J Med Genet; 1984 Jun; 21(3):218-21. PubMed ID: 6431108
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A malformed girl with duplication of chromosome 9q.
    Nakahori Y; Nakagome Y
    J Med Genet; 1984 Oct; 21(5):387-8. PubMed ID: 6502654
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Duplication of 7p: further delineation of the phenotype and restriction of the critical region to the distal part of the short arm.
    Reish O; Berry SA; Dewald G; King RA
    Am J Med Genet; 1996 Jan; 61(1):21-5. PubMed ID: 8741912
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalities.
    Telvi L; Ion A; Carel JC; Desguerre I; Piraud M; Boutin AM; Feingold J; Ponsot G; Fellous M; McElreavey K
    J Med Genet; 1996 Sep; 33(9):767-71. PubMed ID: 8880579
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Developmental abnormalities in a patient with karyotype 46,XX,bq+.
    Chakanovskis JE; Sutherland GR
    J Med Genet; 1970 Jun; 7(2):180-4. PubMed ID: 5519607
    [No Abstract]   [Full Text] [Related]  

  • 29. A cytogenetic survey of mentally retarded children in Taiwan: final report on the incidence of chromosome abnormalities.
    Wuu KD; Wuu SW; Liu IW
    Proc Natl Sci Counc Repub China B; 1984 Jan; 8(1):83-8. PubMed ID: 6531421
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome.
    Jacobs PA; Mayer M; Matsuura J; Rhoads F; Yee SC
    Hum Genet; 1983; 63(2):139-48. PubMed ID: 6840758
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Chromosome 15 abnormality in a mentally retarded adult.
    Kelly S; Almy R; Dagle A
    J Med Genet; 1969 Dec; 6(4):438-41. PubMed ID: 5365954
    [No Abstract]   [Full Text] [Related]  

  • 32. Chromosome abnormalities and Williams-Beuren syndrome.
    Gosch A; Pankau R
    J Med Genet; 1993 Oct; 30(10):886. PubMed ID: 8230171
    [No Abstract]   [Full Text] [Related]  

  • 33. Ring chromosome 18 in a patient with multiple anomalies.
    Palmer CG; Fareed N; Merritt AD
    J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991
    [No Abstract]   [Full Text] [Related]  

  • 34. [Early diagnosis of the trisomy 15q proximialis syndrome].
    Tsancheva MS; Lalov VM; Krachunova MG
    Pediatriia; 1982 Jan; (1):65-6. PubMed ID: 7063327
    [No Abstract]   [Full Text] [Related]  

  • 35. An extra small metacentric chromosome in association with multiple congenital abnormalities.
    Finley WH; Finley SC; Monsky D
    J Med Genet; 1971 Sep; 8(3):381-3. PubMed ID: 5097148
    [No Abstract]   [Full Text] [Related]  

  • 36. Cytogenetic investigations in mentally retarded patients.
    Reddy KS; Thomas IM
    Indian J Med Res; 1985 Aug; 82():164-70. PubMed ID: 4054978
    [No Abstract]   [Full Text] [Related]  

  • 37. A homozygote for pericentric inversion of chromosome 4.
    Carpenter NJ; Say B; Barber ND
    J Med Genet; 1982 Dec; 19(6):469-71. PubMed ID: 6185681
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Williams syndrome and chromosome 18.
    Menko FH; Stouthart PJ
    J Med Genet; 1992 Sep; 29(9):679-80. PubMed ID: 1404306
    [No Abstract]   [Full Text] [Related]  

  • 39. Fragile site at 12q13 associated with phenotypic abnormalities.
    Morić-Petrović S; Laca Z
    J Med Genet; 1984 Jun; 21(3):216-7. PubMed ID: 6748019
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Indications for chromosome analysis illustrated by a case of ring 22.
    Howard-Peebles PN
    J Hered; 1977; 68(4):268-9. PubMed ID: 411817
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.