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 *

109 related articles for article (PubMed ID: 4691557)

  • 21. The electrocardiogram and sex chromosome aneuploidy.
    Price WH; Lauder IJ; Wilson J
    Clin Genet; 1974; 6(1):1-14. PubMed ID: 4426125
    [No Abstract]   [Full Text] [Related]  

  • 22. Children with an XYY sex chromosome constitution.
    Mikel'saar AV; Blyumina MG; Kuznetsova LI; Mikel'saar RV
    Sov Genet; 1973 Dec; 7(8):1074-81. PubMed ID: 4783221
    [No Abstract]   [Full Text] [Related]  

  • 23. The xyy chromosome male--or syndrome?
    Borgaonkar DS; Shah SA
    Prog Med Genet; 1974; 10():135-222. PubMed ID: 4283414
    [No Abstract]   [Full Text] [Related]  

  • 24. Divergent phenotypes among 48,XXXX and 47,XXX females.
    Telfer MA; Richardson CE; Helmken J; Smith GF
    Am J Hum Genet; 1970 May; 22(3):326-35. PubMed ID: 4392739
    [No Abstract]   [Full Text] [Related]  

  • 25. The growth and development of four XYY infants.
    Valentine GH; McClelland MA; Sergovich FR
    Pediatrics; 1971 Oct; 48(4):583-94. PubMed ID: 5114746
    [No Abstract]   [Full Text] [Related]  

  • 26. XXXXY syndrome with mosaicism: case report.
    Gardner RJ; Sands VE; Veale AM; Howarth DA; Parslow MI
    N Z Med J; 1972 Jul; 76(482):22-7. PubMed ID: 4508378
    [No Abstract]   [Full Text] [Related]  

  • 27. A double chromosomal aberration of the 47, XX, 21+-47, XXp-q-, 21+ type in a girl with features of Down's and Turner's syndromes.
    Mikel'saar AV; Blyumina MG; Kuznetsova LI; Mikel'saar RV; Lur'e IV
    Sov Genet; 1971 May; 7(5):675-9. PubMed ID: 4272425
    [No Abstract]   [Full Text] [Related]  

  • 28. A familial Y-autosome translocation in man.
    Noel B; Emerit I; Luciani JM; Quack B
    Clin Genet; 1971; 2(1):1-6. PubMed ID: 5111751
    [No Abstract]   [Full Text] [Related]  

  • 29. A case of 48,XXYY--paternal origin of the extra X chromosome.
    Hillig U; Hoo JJ
    Humangenetik; 1974; 25(2):159-61. PubMed ID: 4442889
    [No Abstract]   [Full Text] [Related]  

  • 30. The indications for chromosome analysis as an aid to the clinician.
    Gordon RR
    Clin Pediatr (Phila); 1968 Feb; 7(2):83-7. PubMed ID: 4229793
    [No Abstract]   [Full Text] [Related]  

  • 31. Analytic review: nature and origin of males with XX sex chromosomes.
    de la Chapelle A
    Am J Hum Genet; 1972 Jan; 24(1):71-105. PubMed ID: 4622299
    [No Abstract]   [Full Text] [Related]  

  • 32. Sex chromosome aneuploidy and criminal behaviour.
    Court Brown WM; Jacobs PA; Price WH
    Eugen Soc Symp; 1968; 4():180-93. PubMed ID: 5761692
    [No Abstract]   [Full Text] [Related]  

  • 33. 49,XXXXX syndrome.
    Fragoso R; Hernandez A; Plascencia ML; Nazara Z; Martinez y Martinez R; Cantu JM
    Ann Genet; 1982; 25(3):145-8. PubMed ID: 6982661
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Case of polysomy X with 49 chromosomes (syndrome 49 XXXXY)].
    Garau A; Crisponi GG; Floris G; Lucia G
    Minerva Pediatr; 1974 Aug; 26(25):1249-59. PubMed ID: 4419085
    [No Abstract]   [Full Text] [Related]  

  • 35. [Clinical features of patients with the syndrome 47, XYY].
    Davidenkova EF; Timofeev NN; Zakharov AM; Kulikov RI; Petrov IA
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1974; 74(9):1369-75. PubMed ID: 4422432
    [No Abstract]   [Full Text] [Related]  

  • 36. [Differentiation of the human X chromosome by length with structural changes present].
    Baranovskaia LI
    Tsitologiia; 1973 Sep; 15(9):1122-9. PubMed ID: 4592863
    [No Abstract]   [Full Text] [Related]  

  • 37. A ring-4 chromosome in a patient with normal intelligence and short stature.
    Surana RB; Bailey JD; Conen PE
    J Med Genet; 1971 Dec; 8(4):517-21. PubMed ID: 5149537
    [No Abstract]   [Full Text] [Related]  

  • 38. The XYY syndrome: reality or myth?
    Noël B; Duport JP; Revil D; Dussuyer I; Quack B
    Clin Genet; 1974; 5(5):387-94. PubMed ID: 4855175
    [No Abstract]   [Full Text] [Related]  

  • 39. Guide to human chromosome defects.
    Redding A; Hirshhorn K
    Birth Defects Orig Artic Ser; 1970 May; 6(1):91-106. PubMed ID: 5522728
    [No Abstract]   [Full Text] [Related]  

  • 40. Conenital hypothyroidism in association with a ring chromosome 18.
    Winter JS; Ahluwalia K; Ray M
    J Med Genet; 1972 Mar; 9(1):122-6. PubMed ID: 5025476
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.