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 *

127 related articles for article (PubMed ID: 6538753)

  • 1. X-linked mental retardation associated with bilateral clasp thumb anomaly.
    Gareis FJ; Mason JD
    Am J Med Genet; 1984 Jan; 17(1):333-8. PubMed ID: 6538753
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mental retardation-clasped thumb syndrome.
    Yeatman GW
    Am J Med Genet; 1984 Jan; 17(1):339-44. PubMed ID: 6538754
    [No Abstract]   [Full Text] [Related]  

  • 3. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation.
    Brooks SS; Wisniewski K; Brown WT
    Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new X-linked mental retardation-overgrowth syndrome.
    Golabi M; Rosen L
    Am J Med Genet; 1984 Jan; 17(1):345-58. PubMed ID: 6538755
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The X-linked syndrome of macroorchidism and mental retardation: further observations.
    Bowen P; Biederman B; Swallow KA
    Am J Med Genet; 1978; 2(4):409-14. PubMed ID: 263449
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A form of X-linked mental retardation with marfanoid habitus.
    Lujan JE; Carlin ME; Lubs HA
    Am J Med Genet; 1984 Jan; 17(1):311-22. PubMed ID: 6711603
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A large kindred with X-linked mental retardation, marker X and macroorchidism.
    Lubs H; Travers H; Lujan E; Carroll A
    Am J Med Genet; 1984 Jan; 17(1):145-57. PubMed ID: 6585140
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism].
    Zollinger A; Schmid W; Vilan J; Sorg B; Knoblauch M
    Schweiz Med Wochenschr; 1983 Feb; 113(7):238-44. PubMed ID: 6836249
    [TBL] [Abstract][Full Text] [Related]  

  • 9. X-linked recessive inheritance of radial ray deficiencies in a family with four affected males.
    Galjaard RJ; Kostakoglu N; Hoogeboom JJ; Breedveld GJ; van der Linde HC; Hovius SE; Oostra BA; Sandkuijl LA; Akarsu AN; Heutink P
    Eur J Hum Genet; 2001 Sep; 9(9):653-8. PubMed ID: 11571552
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Description of a family with 3 brothers with X-linked mental retardation and fragile site Xq 27 der mat].
    Ventruto V; D'Avanzo M; Stabile M; Tolone C; Santinelli R; Dell'Aria V; Toraldo R; De Tollis G
    Pediatria (Napoli); 1983; 91(2-3):241-50. PubMed ID: 6420768
    [No Abstract]   [Full Text] [Related]  

  • 11. A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation.
    Martínez-Garay I; Tomás M; Oltra S; Ramser J; Moltó MD; Prieto F; Meindl A; Kutsche K; Martínez F
    Eur J Hum Genet; 2007 Jan; 15(1):29-34. PubMed ID: 17033686
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?
    Passos-Bueno MR; Byth BC; Rosenberg S; Takata RI; Bakker E; Beggs AH; Pavanello RC; Vainzof M; Davies KE; Zatz M
    Am J Med Genet; 1993 Apr; 46(2):172-5. PubMed ID: 8484404
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Regular dominance of thumb ankylosis with mental retardation transmitted over 3 generations].
    Piussan C; Lenaerts C; Mathieu M; Boudailliez B
    J Genet Hum; 1983 Jun; 31(2):107-14. PubMed ID: 6631421
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage analysis in three families with nonspecific X-linked mental retardation.
    Claes S; Gu XX; Legius E; Lorenzetti E; Marynen P; Fryns JP; Cassiman JJ; Raeymaekers P
    Am J Med Genet; 1996 Jul; 64(1):137-46. PubMed ID: 8826464
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fragile X chromosome and X-linked mental retardation.
    Larbrisseau A; Jean P; Messier B; Richer CL
    Can Med Assoc J; 1982 Jul; 127(2):123-6. PubMed ID: 7093857
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New X-linked mental retardation syndrome with the gene mapped tentatively in Xp22.3.
    Wittwer B; Kircheisen R; Leutelt J; Orth U; Gal A
    Am J Med Genet; 1996 Jul; 64(1):42-9. PubMed ID: 8826447
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Regional localization of two genes for nonspecific X-linked mental retardation to Xp22.3-p22.2 (MRX49) and Xp11.3-p11.21 (MRX50).
    Claes S; Vogels A; Holvoet M; Devriendt K; Raeymaekers P; Cassiman JJ; Fryns JP
    Am J Med Genet; 1997 Dec; 73(4):474-9. PubMed ID: 9415477
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new X-linked syndrome comprising progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness.
    Schimke RN; Horton WA; Collins DL; Therou L
    Am J Med Genet; 1984 Jan; 17(1):323-32. PubMed ID: 6538752
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MCA/MR syndrome with oligodactyly and Möbius anomaly in first cousins: new syndrome or familial facial-limb disruption sequence?
    Journel H; Roussey M; Le Marec B
    Am J Med Genet; 1989 Dec; 34(4):506-10. PubMed ID: 2624259
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new X-linked multiple congenital anomalies/mental retardation syndrome.
    Golabi M; Ito M; Hall BD
    Am J Med Genet; 1984 Jan; 17(1):367-74. PubMed ID: 6711604
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.