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 *

194 related articles for article (PubMed ID: 745219)

  • 1. X-Y translocation in a retarded phenotypic male. Clinical, cytogenetic, biochemical, and serogenetic studies.
    Bernstein R; Wagner J; Isdale J; Nurse GT; Lane AB; Jenkins T
    J Med Genet; 1978 Dec; 15(6):466-74. PubMed ID: 745219
    [TBL] [Abstract][Full Text] [Related]  

  • 2. X;15 translocation in a retarded girl: X inactivation pattern and attempt to localise the hexosaminidase A and other loci.
    Bernstein R; Dawson B; Kohl R; Jenkins T
    J Med Genet; 1979 Aug; 16(4):254-62. PubMed ID: 290816
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation.
    Metaxotou C; Ikkos D; Panagiotopoulou P; Alevizaki M; Mavrou A; Tsenghi C; Matsaniotis N
    Clin Genet; 1983 Nov; 24(5):380-3. PubMed ID: 6652948
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Female phenotype and multiple abnormalities in sibs with a Y chromosome and partial X chromosome duplication: H--Y antigen and Xg blood group findings.
    Bernstein R; Jenkins T; Dawson B; Wagner J; Dewald G; Koo GC; Wachtel SS
    J Med Genet; 1980 Aug; 17(4):291-300. PubMed ID: 7193738
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mental retardation in association with a balanced X-autosome translocation and random inactivation of the X chromosomes.
    Sands ME
    Clin Genet; 1980 May; 17(5):309-16. PubMed ID: 7438488
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Observations in a case of an X/Y translocation, t(X;Y)(p22;q11), in a mother and son.
    Pfeiffer RA
    Cytogenet Cell Genet; 1980; 26(2-4):150-7. PubMed ID: 7389410
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X;Y translocation in an adolescent mentally normal phenotypic male with features of hypogonadism.
    Bernstein R; Pinto MR; Almeida M; Solarsh SM; Meck J; Jenkins T
    J Med Genet; 1980 Dec; 17(6):437-43. PubMed ID: 6937619
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytogenetic studies in a selected group of mentally retarded children.
    Moghe M; Patel ZM; Peter JJ; Ambani LM
    Hum Genet; 1981; 58(2):184-7. PubMed ID: 6456981
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inherited partial X chromosome duplication in a mentally retarded male.
    Nielsen KB; Langkjaer F
    J Med Genet; 1982 Jun; 19(3):222-4. PubMed ID: 7108918
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Translocation of chromosome 4 and 9 with ring formation of chromosome 4 short arm.
    Bernstein R; Milne AT; Jenkins T
    J Med Genet; 1978 Aug; 15(4):310-4. PubMed ID: 712764
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation.
    Palka-Bayard-de-Volo C; De Marco S; Chiavaroli V; Alfonsi M; Calabrese G; Chiarelli F; Mohn A
    Gene; 2012 Aug; 504(1):107-10. PubMed ID: 22583828
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a 650 kb duplication at the X chromosome breakpoint in a patient with 46,X,t(X;8)(q28;q12) and non-syndromic mental retardation.
    Cox JJ; Holden ST; Dee S; Burbridge JI; Raymond FL
    J Med Genet; 2003 Mar; 40(3):169-74. PubMed ID: 12624134
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A possible exception to the critical region hypothesis.
    Barnabei VM; Wyandt HE; Kelly TE
    Am J Hum Genet; 1981 Jan; 33(1):61-6. PubMed ID: 7468594
    [TBL] [Abstract][Full Text] [Related]  

  • 14. X/Y translocation in a family with X-linked ichthyosis, chondrodysplasia punctata, and mental retardation: DNA analysis reveals deletion of the steroid sulphatase gene and translocation of its Y pseudogene.
    Ballabio A; Parenti G; Carrozzo R; Coppa G; Felici L; Migliori V; Silengo M; Franceschini P; Andria G
    Clin Genet; 1988 Jul; 34(1):31-7. PubMed ID: 3165728
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation.
    Leisti JT; Kaback MM; Rimoin DL
    Am J Hum Genet; 1975 Jul; 27(4):441-53. PubMed ID: 1155455
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genetic study of a child carrying a maternally derived unbalanced 46,Y,der(X)t(X;Y)(p22;q11) chromosomal translocation].
    Yin T; Wang Y; Wang Z; Zhang R; Wang L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Apr; 38(4):376-379. PubMed ID: 33834470
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A cytogenetic survey of an institution for the mentally retarded: I. Chromosome abnormalities.
    Jacobs PA; Matsuura JS; Mayer M; Newlands IM
    Clin Genet; 1978 Jan; 13(1):37-60. PubMed ID: 146575
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/46,XX,r(22)/46,XX karyotype in the mother.
    Fryns JP; Van den Berghe H
    Hum Genet; 1979 Mar; 47(2):213-6. PubMed ID: 437787
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype.
    Magenis RE; Webb MJ; McKean RS; Tomar D; Allen LJ; Kammer H; Van Dyke DL; Lovrien E
    Hum Genet; 1982; 62(3):271-6. PubMed ID: 6892019
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal height.
    Spranger S; Kirsch S; Mertz A; Schiebel K; Tariverdian G; Rappold GA
    Clin Genet; 1997 May; 51(5):346-50. PubMed ID: 9212185
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.