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 *

95 related articles for article (PubMed ID: 4824840)

  • 21. [Dermatoglyphics in Turner's syndrome (45,X). Comparison of results with those of a normal urban Mexican population].
    Armendares S; Jiménez AM; Cantú JM
    Rev Invest Clin; 1972; 24(2):139-45. PubMed ID: 5055513
    [No Abstract]   [Full Text] [Related]  

  • 22. [The chromsomes in human pathology].
    PERICOLI DF
    Policlinico Prat; 1962 Feb; 69():193-216. PubMed ID: 14038278
    [No Abstract]   [Full Text] [Related]  

  • 23. [Pericentric inversions of chromosomes 1, 9 and 16 in patients with sex chromosome anomalies].
    Verlinskaia DK; Prozorova MV; Khitrikov LE
    Tsitol Genet; 1982; 16(1):57-60. PubMed ID: 7064223
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Sexual differentiation.
    King CR; Pernoll ML
    Obstet Gynecol Annu; 1984; 13():1-33. PubMed ID: 6371611
    [No Abstract]   [Full Text] [Related]  

  • 25. [Dermatoglyphics in Klinefelter's disease].
    Verlinskaia DK; Ponomarenko AM
    Vopr Psikhiatr Nevropatol; 1968; 13():134-7. PubMed ID: 5740999
    [No Abstract]   [Full Text] [Related]  

  • 26. Genes and chromosomes. Part 4--Genetic anomalies and disorders.
    Nigam Y; Bexfield A
    Nurs Times; 2008 Jul 1-7; 104(26):24-5. PubMed ID: 18669399
    [No Abstract]   [Full Text] [Related]  

  • 27. Genetics: the shape of things to come.
    Cowie V
    Nurs Mirror; 1979 Dec; 149(23):22-4. PubMed ID: 260179
    [No Abstract]   [Full Text] [Related]  

  • 28. [Xg-blood group system. A review].
    Froland A
    Ugeskr Laeger; 1967 May; 129(20):651-4. PubMed ID: 4877698
    [No Abstract]   [Full Text] [Related]  

  • 29. Diagnostic significance of dermatoglyphics in certain birth defects.
    Temtamy SA; El-Mazni A; Hussien FH; Salam MA; Moussa AA; Zaki ME; El Meniawi LE
    Prog Clin Biol Res; 1982; 84():393-420. PubMed ID: 7100198
    [No Abstract]   [Full Text] [Related]  

  • 30. [Sex differentiation and its disorders].
    Engel W
    Verh Dtsch Ges Pathol; 1982; 66():329-43. PubMed ID: 7184256
    [No Abstract]   [Full Text] [Related]  

  • 31. [Gonadal dysgenesis].
    Delgado A; Molina M
    An Esp Pediatr; 1983 Sep; 19 Suppl 18():161-77. PubMed ID: 6651009
    [No Abstract]   [Full Text] [Related]  

  • 32. Chromosomal syndromes.
    Temple MJ
    Hosp Pract (Off Ed); 1983 Feb; 18(2):124A, 124D, 124F passim. PubMed ID: 6218063
    [No Abstract]   [Full Text] [Related]  

  • 33. Some contributions of blood groups to human genetics.
    Sanger R; Racew RR
    Am J Clin Pathol; 1971 Jun; 55(6):635-45. PubMed ID: 5567016
    [No Abstract]   [Full Text] [Related]  

  • 34. Some contributions of blood groups to human genetics.
    Sanger R; Race RR
    Am J Clin Pathol; 1971 Jun; 55(6):635-45. PubMed ID: 4937172
    [No Abstract]   [Full Text] [Related]  

  • 35. Infertility and chromosome abnormality.
    Chandley AC
    Oxf Rev Reprod Biol; 1984; 6():1-46. PubMed ID: 6397710
    [No Abstract]   [Full Text] [Related]  

  • 36. Developmental disorders of the lymphatic system.
    Greenlee R; Hoyme H; Witte M; Crowe P; Witte C
    Lymphology; 1993 Dec; 26(4):156-68. PubMed ID: 8121193
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Hermaphroditism.
    Snyder CC
    Clin Plast Surg; 1980 Apr; 7(2):179-96. PubMed ID: 7398198
    [No Abstract]   [Full Text] [Related]  

  • 38. [Dermatoglyphics in gonadal dysgeneses of masculine and feminine phenotypes].
    Málková J
    Cesk Pediatr; 1970 Apr; 25(4):176-9. PubMed ID: 5444507
    [No Abstract]   [Full Text] [Related]  

  • 39. [Klinefelter's syndrome. Karyotype XXYY. Study of dermatoglyphics].
    Muller JM; Jalbert P; Cordonnier D
    Ann Biol Clin (Paris); 1967; 25(1):207-14. PubMed ID: 6031413
    [No Abstract]   [Full Text] [Related]  

  • 40. Is there an influence of X-chromosomal imprinting on the phenotype in Klinefelter syndrome? A clinical and molecular genetic study of 61 cases.
    Stemkens D; Roza T; Verrij L; Swaab H; van Werkhoven MK; Alizadeh BZ; Sinke RJ; Giltay JC
    Clin Genet; 2006 Jul; 70(1):43-8. PubMed ID: 16813603
    [TBL] [Abstract][Full Text] [Related]  

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