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 *

70 related articles for article (PubMed ID: 5041046)

  • 21. Family with partial monosomy 10p and trisomy 10p.
    Hon E; Chapman C; Gunn TR
    Am J Med Genet; 1995 Mar; 56(2):136-40. PubMed ID: 7625434
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)].
    Rethoré MO; Lafourcade J; Couturier J; Harpey JP; Hamet M; Engler R; Alcindor LG; Lejeune J
    Ann Genet; 1982; 25(1):36-42. PubMed ID: 6979298
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Partial trisomy 20p: familial occurrence.
    Oppenheimer S; Dignan P; Soukup S
    Am J Med Genet; 2000 Dec; 95(4):316-9. PubMed ID: 11186883
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Partial trisomy 18 (pter leads to q122) of maternal origin (author's transl)].
    Jaffray JY; Geneix A; Goumy P; Perissel B; Menut G; Malet P
    Ann Genet; 1980; 23(4):224-7. PubMed ID: 6971601
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].
    Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V
    Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734
    [No Abstract]   [Full Text] [Related]  

  • 26. Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7p due to a de novo tandem duplication 7 (p15.1-->p21.3).
    Kleczkowska A; Decock P; van den Berghe H; Fryns JP
    Genet Couns; 1994; 5(4):393-7. PubMed ID: 7888144
    [No Abstract]   [Full Text] [Related]  

  • 27. [Mental retardation in the crying cat syndrome. Comparison of the intellectual level in the partial deletion of the short arm of chromosome 5 with trisomy 21 and deletions of chromosome 18. Apropos of 118 cases taken from the literature].
    Moor L
    Rev Neuropsychiatr Infant; 1968 Mar; 16(3):257-67. PubMed ID: 5683042
    [No Abstract]   [Full Text] [Related]  

  • 28. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)].
    Obry E; Piussan C; Risbourg B; Dutrillaux B
    Ann Genet; 1980; 23(4):216-20. PubMed ID: 6971599
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Trisomy 17-18 or E-trisomy].
    Sauer O
    Kinderarztl Prax; 1970 May; 38(5):213-8. PubMed ID: 5483879
    [No Abstract]   [Full Text] [Related]  

  • 30. An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree.
    Smith GF; Shear CS; Jalowayski I; Akesson HO
    J Ment Defic Res; 1969 Jun; 13(2):123-9. PubMed ID: 5794286
    [No Abstract]   [Full Text] [Related]  

  • 31. Partial trisomy 1q and monosomy 18q due to a de novo t(1;18)(q25;q23).
    Solé MT; Rivera H; Sánchez-Corona J; Plascencia L; Cantú JM
    Ann Genet; 1983; 26(2):120-2. PubMed ID: 6604487
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Association of trisomy 21 and gonosomal trisomy. Apropos of 2 cases].
    Castel Y; Le Marec B; Toudic L; Lemarchand M; Cosson JP
    Pediatrie; 1983 Jun; 38(4):235-41. PubMed ID: 6225989
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Phenotype signs at different ages in partial trisomy 3p by familial translocation 3/5].
    Schwanitz G; Zerres K
    Ann Genet; 1984; 27(3):167-72. PubMed ID: 6334481
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Apropos of trisomy 18 - a study of 4 observations].
    Gilgenkrantz S; Sapelier J; Thiriet M; Kahn C; Pierson M
    Ann Genet; 1967 Mar; 10(1):32-8. PubMed ID: 5300124
    [No Abstract]   [Full Text] [Related]  

  • 35. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.
    Littooij AS; Hochstenbach R; Sinke RJ; van Tintelen P; Giltay JC
    Am J Med Genet; 2002 Apr; 109(2):125-32. PubMed ID: 11977161
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Trisomy 18 (Edwards syndrome) in Delaware.
    Morallo LM; Rosenblum H; Esterly KL; Johnson WD; Storlazzi JJ; Narvaez AC; Borgaonkar DS
    Del Med J; 1983 Jan; 55(1):27-30. PubMed ID: 6840358
    [No Abstract]   [Full Text] [Related]  

  • 37. [Trisomy 18 with prolonged survival. Case report of a girl followed to 6 years of age].
    Roussey M; Le Marec B; Le Berre C; Le Mée F; Picard F; Sénécal J
    Pediatrie; 1979 Dec; 34(8):819-26. PubMed ID: 545280
    [No Abstract]   [Full Text] [Related]  

  • 38. [On three cases of C trisomy].
    Lejeune J; Dutrillaux B; Rethoré MO; Berger R; Debray H; Veron P; Gorce F; Grossiord A
    Ann Genet; 1969 Mar; 12(1):28-35. PubMed ID: 5306709
    [No Abstract]   [Full Text] [Related]  

  • 39. [Trisomy 18. Case report].
    Zanetti P; De Sanctis C
    Minerva Pediatr; 1969 Oct; 21(41):1910-5. PubMed ID: 5391364
    [No Abstract]   [Full Text] [Related]  

  • 40. Partial trisomy of chromosome 3(p14----p22) due to maternal insertional translocation.
    Kleczkowska A; Fryns JP; Van den Berghe H
    Ann Genet; 1984; 27(3):180-3. PubMed ID: 6334484
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.