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 *

91 related articles for article (PubMed ID: 4671773)

  • 21. [Chromosome aberrations in ophthalmology].
    François J; Berger R; Saraux H
    Bull Mem Soc Fr Ophtalmol; 1972; 85(0):1-37. PubMed ID: 4671737
    [No Abstract]   [Full Text] [Related]  

  • 22. [Chromosome study in complete universal albinism with nystagmus].
    Balacco-Gabrieli C; Guanti G
    Ann Ocul (Paris); 1969 May; 202(5):463-8. PubMed ID: 5368971
    [No Abstract]   [Full Text] [Related]  

  • 23. [The Dr phenotype: a study of threee cases with a ring D chromosome].
    Lejeune J; Lafourcade J; Berger R; Cruveiller J; Rethoré MO; Dutrillaux B; Abonyi D; Jérôme H
    Ann Genet; 1968 Jun; 11(2):79-87. PubMed ID: 5303427
    [No Abstract]   [Full Text] [Related]  

  • 24. [18p- syndrome. A further case].
    Ayraud N; Darcourt G; D'Oelsnitz M; Poujol J; Lavagna J; Capdeville C
    Ann Genet; 1969 Jun; 12(2):122-5. PubMed ID: 5308384
    [No Abstract]   [Full Text] [Related]  

  • 25. Partial trisomy of chromosome 11: a case report.
    Falk RE; Carrel RE; Valente M; Crandall BF; Sparkes RS
    Am J Ment Defic; 1973 Jan; 77(4):383-8. PubMed ID: 4706396
    [No Abstract]   [Full Text] [Related]  

  • 26. Second case of chromosomal translocation t(4p 14q) (in a boy with severe kyphoscoliosis and obesity of the trunk).
    Geib K; Pfeiffer RA
    Ann Genet; 1969 Jun; 12(2):115-8. PubMed ID: 5308382
    [No Abstract]   [Full Text] [Related]  

  • 27. [New documents of delineation of a syndrome of the deletion of the short arm of one chromosome no 4].
    Pfeiffer RA
    Z Kinderheilkd; 1968; 102(1):49-61. PubMed ID: 5303548
    [No Abstract]   [Full Text] [Related]  

  • 28. [A human chromosome translocation from the eighteenth century].
    Stalder GR; Bühler EM
    Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg; 1967; 41(2-4):87-93. PubMed ID: 5631509
    [No Abstract]   [Full Text] [Related]  

  • 29. [Deficiency in the short arms of Group B (4p--; 5p--) chromosomes. Studies on 6 patients].
    Altrogge HC; Hirth L; Goedde HW; Schroeder HJ
    Z Kinderheilkd; 1971; 110(3):218-47. PubMed ID: 5088755
    [No Abstract]   [Full Text] [Related]  

  • 30. [Anomaly of chromosomic structure (46,XX,17q+) in a polymalformed child].
    Walbaum R; Dupuis C; Dehaene P; Delmas-Marsalet Y
    Ann Genet; 1968 Mar; 11(1):53-5. PubMed ID: 5301757
    [No Abstract]   [Full Text] [Related]  

  • 31. [The deletion of the short arm of chromosome 18 (18p- syndrome), apropos of a new observation].
    Gilgenkrantz S; Marchal C; Neimann N
    Ann Genet; 1968 Mar; 11(1):17-21. PubMed ID: 5301751
    [No Abstract]   [Full Text] [Related]  

  • 32. Cri-du-chat syndrome. Case report.
    Schmid W; Vischer D
    Helv Paediatr Acta; 1967 Apr; 22(1):22-7. PubMed ID: 5585045
    [No Abstract]   [Full Text] [Related]  

  • 33. Subglottic pseudotumor, laryngeal dysplasia, and chondrodysplasia calcificans congenita with a t(D;B) chromosomal translocation.
    Valdmanis A; Wilson JR; Mann JD; Pearson G; Shaw MW
    Ann Genet; 1967 Jun; 10(2):55-9. PubMed ID: 5298973
    [No Abstract]   [Full Text] [Related]  

  • 34. A family with balanced translocation, t(5p-;Gp+).
    White BJ; Van de Water LC; Tjio J
    J Med Genet; 1971 Jun; 8(2):188-94. PubMed ID: 5096542
    [No Abstract]   [Full Text] [Related]  

  • 35. [Segregation of a balanced translocation t(5p-;Gp+)].
    Noel B; Quack B; Thiriet M
    Ann Genet; 1968 Dec; 11(4):247-52. PubMed ID: 5306368
    [No Abstract]   [Full Text] [Related]  

  • 36. [Coloboma and anal atresia: phenotype of a chromosome aberration?].
    Pfeiffer RA; Heimann K; Heiming E; Schlack H; Maul H
    Klin Monbl Augenheilkd; 1971 Sep; 159(3):357-67. PubMed ID: 5003627
    [No Abstract]   [Full Text] [Related]  

  • 37. Enlargement of the long arm of a B-group chromosome (Bq+) in a boy aged nine years.
    Revazov AA; Derilo TG; Vorsanova SG
    Sov Genet; 1973 Dec; 7(8):1086-9. PubMed ID: 4783223
    [No Abstract]   [Full Text] [Related]  

  • 38. [Trisomy due to transmitted translocation t(13 q , 14 q ). Estimation of recurrence risks].
    Belaisch G; Despres P; Plainfosse B; Rethore O; Emerit I; Loewe-Lyon S; Lejeune J; Seringe P
    Arch Fr Pediatr; 1971 Oct; 28(8):865-74. PubMed ID: 5123542
    [No Abstract]   [Full Text] [Related]  

  • 39. [Genetic counseling. Apropos of familial transmission of 21-D translocation].
    Attal B; Cottin J; Someily I
    Bull Fed Soc Gynecol Obstet Lang Fr; 1971; 23(4):494-7. PubMed ID: 5153258
    [No Abstract]   [Full Text] [Related]  

  • 40. [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]  

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