BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 19929089)

  • 21. [Cytogenetic studies in Klinefelter's syndrome with 47,XXY-48,XXXY karyotype].
    Kaluzewski B; Jezewska-Musial M; Moruzgala T
    Endokrynol Pol; 1972; 23(3):267-81. PubMed ID: 5069704
    [No Abstract]   [Full Text] [Related]  

  • 22. Monozygotic twins with 45,X/46,XY mosaicism discordant for phenotypic sex.
    Costa T; Lambert M; Teshima I; Ray PN; Richer CL; Dallaire L
    Am J Med Genet; 1998 Jan; 75(1):40-4. PubMed ID: 9450855
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Novel isodicentric chromosome 18 in an abnormal infant with a mosaic karyotype [46,XY/46,XY,-18,+dic(18)(q12.2]).
    Bryke CR; Lindgren V; Fryburg JS; Yang-Feng TL
    Am J Med Genet; 1990 Jun; 36(2):247-50. PubMed ID: 2368814
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A rare variant Klinefelter syndrome seen 40 years later: 47,X,del(Xq24),Y.
    Özkent MS; Balasar Ö
    Andrologia; 2021 Dec; 53(11):e14213. PubMed ID: 34375016
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
    Habecker-Green JG; Naeem R; Gold H; O'Grady JP; Kanaan C; Bayer-Zwirello L; Murray MS; Cohn GM
    J Perinatol; 1998; 18(5):395-8. PubMed ID: 9766419
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Cytogenetic study of 257 mentally deficient patients in psychiatric hospitals].
    Bourgeois M; Bénézech M; Tournier-Zerbid N; Constant-Boy M; Benazet-Rissou J
    Ann Med Psychol (Paris); 1975 Nov; 2(4):756-82. PubMed ID: 135524
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cleft palate in Kabuki syndrome: a report of six cases.
    Iida T; Park S; Kato K; Kitano I
    Cleft Palate Craniofac J; 2006 Nov; 43(6):756-61. PubMed ID: 17105332
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cleft-palate lateral synechia syndrome: insight into the phenotypic spectrum of Fryns syndrome?
    Jaeger A; Kapur R; Whelan M; Leung E; Cunningham M
    Birth Defects Res A Clin Mol Teratol; 2003 Jun; 67(6):460-6. PubMed ID: 12962292
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Infertility and multiple urogenital abnormalities in a male with mosaic 46,XY/45,XO/47,XXY karyotype and mixed phenotype.
    Filiadis IF; Syrrou MB; Bai MC; Georgiou IA; Pagoulatos GN; Giannakopoulos X
    Urol Int; 1998; 61(2):111-4. PubMed ID: 9873251
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Triple chromosomal mosaicism XY-XXY-XXxY in Klinefelter's syndrome.
    Hsu LY; Geller J; Nemhauser I
    J Clin Endocrinol Metab; 1966 Jan; 26(1):104-10. PubMed ID: 5901592
    [No Abstract]   [Full Text] [Related]  

  • 31. Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant.
    Höckner M; Pinggera GM; Günther B; Sergi C; Fauth C; Erdel M; Kotzot D
    Fertil Steril; 2008 Nov; 90(5):2009.e13-7. PubMed ID: 18687426
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A case of a rare variant of Klinefelter syndrome, 47,XY,i(X)(q10).
    Kondo T; Kuroda S; Usui K; Mori K; Asai T; Takeshima T; Kawahara T; Hamanoue H; Uemura H; Yumura Y
    Andrologia; 2018 Sep; 50(7):e13024. PubMed ID: 29665107
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Tissue-limited mosaicism in Pallister-Killian syndrome -- a case in point.
    Choo S; Teo SH; Tan M; Yong MH; Ho LY
    J Perinatol; 2002; 22(5):420-3. PubMed ID: 12082482
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Is the male Aicardi's characterized by 46 XXY karyotype?
    Saddichha S
    J Neurol Sci; 2009 Sep; 284(1-2):222; author reply 222. PubMed ID: 19359000
    [No Abstract]   [Full Text] [Related]  

  • 35. A simple screening method for detection of Klinefelter syndrome and other X-chromosome aneuploidies based on copy number of the androgen receptor gene.
    Ottesen AM; Garn ID; Aksglaede L; Juul A; Rajpert-De Meyts E
    Mol Hum Reprod; 2007 Oct; 13(10):745-50. PubMed ID: 17720778
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Study of meiotic chromosomes in a caseof Klinefelter'sdisease with spermatogenesis and 46,XY-47,XXY karyotype.
    Luciani JM; Mattei A; Devictor-Vuillet M; Rubin ; Stahl A; Vague J
    Ann Genet; 1970 Dec; 13(4):249-53. PubMed ID: 5313388
    [No Abstract]   [Full Text] [Related]  

  • 37. Palatal and alveolar arch dimensions in 47,XXY (Klinefelter syndrome) men.
    Laine T; Alvesalo L
    Hum Biol; 1993 Feb; 65(1):131-8. PubMed ID: 8436386
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood: trisomy 9 mosaicism.
    Kosaki R; Hanai S; Kakishima H; Okada MA; Hayashi S; Ito Y; Takahashi T; Kosaki K; Okuyama T
    Congenit Anom (Kyoto); 2006 Jun; 46(2):115-7. PubMed ID: 16732770
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Nekrozoospermia in mosaic Klinefelter's syndrome.
    Leipoldt M; Eiben B; Krause W; Engel W
    Andrologia; 1987; 19(2):175-7. PubMed ID: 3688486
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Syndrome of cleft palate, microcephaly, large ears, and short stature (Say syndrome).
    Abu-Libdeh B; Fujimoto A; Ehinger M
    Am J Med Genet; 1993 Feb; 45(3):358-60. PubMed ID: 8434624
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.