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: 4834988)

  • 41. Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease.
    Noonan JA
    Am J Dis Child; 1968 Oct; 116(4):373-80. PubMed ID: 4386970
    [No Abstract]   [Full Text] [Related]  

  • 42. [Skeletal changes in congenital dysgenesis of the ovary (a report of 10 cases)].
    Lang ZJ
    Zhonghua Fang She Xue Za Zhi; 1985 Aug; 19(4):229-31. PubMed ID: 2932316
    [No Abstract]   [Full Text] [Related]  

  • 43. Associated acral and renal malformations: a new syndrome?
    Curran AS; Curran JP
    Pediatrics; 1972 May; 49(5):716-25. PubMed ID: 4402497
    [No Abstract]   [Full Text] [Related]  

  • 44. Anomalies of development in a girl with unusual sex chromosomal mosaicism.
    Thorburn MJ; Miller CG; Dovey P
    J Med Genet; 1967 Dec; 4(4):283-7. PubMed ID: 6082908
    [No Abstract]   [Full Text] [Related]  

  • 45. Ring chromosome 18 in a patient with multiple anomalies.
    Palmer CG; Fareed N; Merritt AD
    J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991
    [No Abstract]   [Full Text] [Related]  

  • 46. Congenital dislocation of the knees in a child with Down-mosaic Turner syndrome.
    Gatrad AR
    J Med Genet; 1981 Apr; 18(2):148-51. PubMed ID: 6453997
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Mosaicism in Shereshevskiĭ-Turner's syndrome: clinical manifestations and dermatoglyphic characteristics].
    Egorkina DA; Gurevich LE; Tomadze AA
    Sov Med; 1984; (4):43-8. PubMed ID: 6740399
    [No Abstract]   [Full Text] [Related]  

  • 48. Radiologic seminar. CXXIV. Gonadal dysgenesis.
    Gibson JY
    J Miss State Med Assoc; 1973 Feb; 14(2):50-1. PubMed ID: 4687172
    [No Abstract]   [Full Text] [Related]  

  • 49. [Translocation D-D and Turner's syndrome. Considerations on a rare association of chromosome pathology].
    Giovannucci ML; Pierro U; Cordelli F; Paoli A
    Haematologica; 1969; 54(11):813-26. PubMed ID: 4993250
    [No Abstract]   [Full Text] [Related]  

  • 50. [X-ray study on congenital gonadal dysgenesis (Turner's syndrome)].
    Zhang XZ; Zhou FX; Chen Y
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1983 Feb; 5(1):43-6. PubMed ID: 6226385
    [No Abstract]   [Full Text] [Related]  

  • 51. Isochromosome Xpi; diagnosis and phenotypic expression.
    Kirillova EA; Zolotukhina TV; Mikel'saar AV; Seleznev YuV ; Rozovskii IS
    Sov Genet; 1974 May; 8(3):370-7. PubMed ID: 4846481
    [No Abstract]   [Full Text] [Related]  

  • 52. [Pure familial gonadal dysgenesis].
    Berger R; Binoux M; Chassan E; Lejeune J
    Ann Endocrinol (Paris); 1972; 33(1):35-40. PubMed ID: 4657311
    [No Abstract]   [Full Text] [Related]  

  • 53. [Phenotype of Turner in the boy: clinical, cytogenetic and dermatoglyphic study].
    Ferrier PE; Ferrier SA
    Union Med Can; 1968 Jul; 97(7):924-8. PubMed ID: 5715601
    [No Abstract]   [Full Text] [Related]  

  • 54. Skeletal measurement in the evaluation of congenital malformation syndromes.
    Poznanski AK; Garn SM
    Birth Defects Orig Artic Ser; 1974; 10(9):125-38. PubMed ID: 4278674
    [No Abstract]   [Full Text] [Related]  

  • 55. [Radiomorphometric skeletal study in the differential diagnosis of endocrine dwarfism in children].
    Preden N; Bannert N; Keller E; Mohnike K
    Padiatr Grenzgeb; 1984; 23(6):367-75. PubMed ID: 6533536
    [No Abstract]   [Full Text] [Related]  

  • 56. [Statistical analysis of the number of karyotypes to be examined in order to diagnose a Turner patient (45, XO) and the number necessary to differentiate the Turner (45, XO) from a mosaic patient (45, OX/46, XX) (author's transl)].
    Arita S; Namba M
    Rinsho Byori; 1979 Dec; 27(12):1087-90. PubMed ID: 541855
    [No Abstract]   [Full Text] [Related]  

  • 57. [Familial character of Shereshevskiĭ-Turner syndrome with karyotype 45, XO-46, XX].
    Rakhal'skiĭ IuE; Sirovskiĭ AA
    Probl Endokrinol (Mosk); 1970; 16(3):44-5. PubMed ID: 5513845
    [No Abstract]   [Full Text] [Related]  

  • 58. Turner's syndrome and 46,X,i(Yq) karyotype.
    Magnelli NC; Vianna-Morgante AM; Frota-Pessoa O; Taboada-Lopez MG
    J Med Genet; 1974 Dec; 11(4):403-6. PubMed ID: 4443992
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Direct familial transmission of the Turner phenotype.
    Nora JJ; Sinha AK
    Am J Dis Child; 1968 Oct; 116(4):343-50. PubMed ID: 5697967
    [No Abstract]   [Full Text] [Related]  

  • 60. Ring-G chromosome, a new G-deletion syndrome?
    Weleber RG; Hecht F; Giblett ER
    Am J Dis Child; 1968 Apr; 115(4):489-93. PubMed ID: 4296014
    [No Abstract]   [Full Text] [Related]  

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