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 *

150 related articles for article (PubMed ID: 4125989)

  • 21. Deletion of the short arm of chromosome No. 10.
    Shokeir MH; Ray M; Hamerton JL; Bauder F; O'Brien H
    J Med Genet; 1975 Mar; 12(1):99-103. PubMed ID: 47396
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Partial deletion of long arms of chromosome 18.
    Kushnick T; Matsushita G
    Pediatrics; 1968 Jul; 42(1):194-7. PubMed ID: 5657675
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. [A small supernumerary metacentric chromosome: interprétation test (author's transl)].
    Ayraud N; Noel B; Llyod M; Letourneau J; Martinon J
    J Genet Hum; 1976 Jun; 24(2):81-93. PubMed ID: 965953
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression].
    Frankova YE; Holenova H; Braulke I
    Monatsschr Kinderheilkd; 1991 Dec; 139(12):841-3. PubMed ID: 1770961
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Presumptive mosaic partial trisomy associated with congenital anomalies and mental deficiency.
    Vianna-Morgante AM; Domingues WM; Ortega CC; Kasahara S
    J Med Genet; 1974 Mar; 11(1):104-8. PubMed ID: 4134623
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Report of five unrelated patients with a small, metacentric, extra chromosome or fragment.
    Borgaonkar S; Schimke RN; Thomas H
    J Genet Hum; 1971 Sep; 19(3):207-22. PubMed ID: 5150016
    [No Abstract]   [Full Text] [Related]  

  • 28. Probable pericentric inversion in chromosome no. 1 in a female child (46,XX,inv(Ip+q-).
    Mikelsaar AV; Ananjev EV; Gindilis VM
    Humangenetik; 1970; 9(4):316-24. PubMed ID: 5449945
    [No Abstract]   [Full Text] [Related]  

  • 29. Trisomy 18 syndrome in Chinese infants. Clinical findings and incidence.
    Emanuel I; Huang SW; Chiang WT; Yang CP
    J Med Genet; 1970 Jun; 7(2):138-41. PubMed ID: 5519599
    [No Abstract]   [Full Text] [Related]  

  • 30. Trisomy 17p due to A t(5;17) (p15;p11) pat translocation.
    Jinno Y; Matsuda I; Kajii T
    Ann Genet; 1982; 25(2):123-5. PubMed ID: 6984629
    [TBL] [Abstract][Full Text] [Related]  

  • 31. An extra small metacentric autosome in a mentally retarded boy with multiple malformations.
    Armendares S; Buentello L; Salamanca F
    J Med Genet; 1971 Sep; 8(3):378-80. PubMed ID: 5097147
    [No Abstract]   [Full Text] [Related]  

  • 32. Trisomy 22 and facioauriculovertebral (Goldenhar) sequence.
    Kobrynski L; Chitayat D; Zahed L; McGregor D; Rochon L; Brownstein S; Vekemans M; Albert DL
    Am J Med Genet; 1993 Apr; 46(1):68-71. PubMed ID: 8494034
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [A case of Patau syndrome. Fetal heart defect and lip-jaw-palate cleft as indicators].
    Küffer E; Asseryanis E; Eppel W; Schurz B; Reinold E
    Ultraschall Med; 1994 Aug; 15(4):217-8. PubMed ID: 7973594
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Anophthalmia with cleft palate and micrognathia: a new syndrome?
    Phadke SR; Sharma AK; Agarwal SS
    J Med Genet; 1994 Dec; 31(12):960-1. PubMed ID: 7891380
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Brother and sister with trisomy 10p: a new syndrome.
    Schleiermacher E; Schliebitz U; Steffens C
    Humangenetik; 1974; 23(3):163-72. PubMed ID: 4844639
    [No Abstract]   [Full Text] [Related]  

  • 36. 48,XXX, plus 18 double trisomy.
    Madahar DP; Dosik H; Wexler I
    J Med Genet; 1974 Sep; 11(3):309-11. PubMed ID: 4139265
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Oro-palatal dysplasia Bettex-Graf--a new syndrome.
    Bettex M; Graf B; Winkler B; Gerber-Huber S
    Eur J Pediatr Surg; 1998 Feb; 8(1):4-8. PubMed ID: 9550268
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Further studies on the genetic heterogeneity of cebocephaly.
    Lazjuk GI; Lurie IW; Nedzved MK
    J Med Genet; 1976 Aug; 13(4):314-8. PubMed ID: 957381
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fetal facial defects: associated malformations and chromosomal abnormalities.
    Nicolaides KH; Salvesen DR; Snijders RJ; Gosden CM
    Fetal Diagn Ther; 1993; 8(1):1-9. PubMed ID: 8452644
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of 21r and 22r chromosomes by quinacrine fluorescence.
    Crandall BF; Weber F; Muller HM; Burwell JK
    Clin Genet; 1972; 3(4):264-70. PubMed ID: 5054320
    [No Abstract]   [Full Text] [Related]  

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