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 *

83 related articles for article (PubMed ID: 1005807)

  • 21. MEHMO (mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly, obesity), a novel syndrome: assignment of disease locus to xp21.1-p22.13.
    Steinmüller R; Steinberger D; Müller U
    Eur J Hum Genet; 1998; 6(3):201-6. PubMed ID: 9781023
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Rud syndrome].
    Kuniba H; Egashira M; Motomura H; Motomura K; Kondoh T
    Nihon Rinsho; 2006 Sep; Suppl 3():485-7. PubMed ID: 17022593
    [No Abstract]   [Full Text] [Related]  

  • 23. [Seizures-ichthyosis-mental retardation].
    Ito M; Sugie H
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):622. PubMed ID: 11528930
    [No Abstract]   [Full Text] [Related]  

  • 24. MENTAL RETARDATION: METHODS OF DIAGNOSIS AND SOME RECENTLY DESCRIBED SYNDROMES.
    RICHARDS BW
    Can Med Assoc J; 1963 Nov; 89(20):1024-9. PubMed ID: 14081787
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [The chromosomal pathology as a contribution to a genetically oriented psychiatry].
    Haberlandt WF
    Nervenarzt; 1966 Feb; 37(2):45-51. PubMed ID: 4226918
    [No Abstract]   [Full Text] [Related]  

  • 26. Rud syndrome. A case report.
    Franzoni E; Lambertini A; Scanabissi E
    Ital J Neurol Sci; 1981 Dec; 2(4):399-401. PubMed ID: 7333832
    [No Abstract]   [Full Text] [Related]  

  • 27. [Rud's syndrome].
    Avendaño I; Aspillaga M
    Rev Chil Pediatr; 1986; 57(6):569-70. PubMed ID: 3671837
    [No Abstract]   [Full Text] [Related]  

  • 28. A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophy.
    Stoll C; Eyer D
    Ann Genet; 1999; 42(1):45-50. PubMed ID: 10214507
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Sjögren-Larsson syndrome. Study of 2 cases].
    Cabezuelo-Huerta G; Mulas F; Frontera-Izquierdo P
    An Esp Pediatr; 1983 May; 18(5):399-402. PubMed ID: 6614675
    [TBL] [Abstract][Full Text] [Related]  

  • 30. MEHMO, a novel syndrome: assignment of disease locus to Xp21.1-p22.13. Mental retardation, epileptic seizures, hypogonadism and genitalism, microcephaly, obesity.
    DeLozier-Blanchet CD; Haenggeli CA; Bottani A
    Eur J Hum Genet; 1999 Sep; 7(6):621-2. PubMed ID: 10482947
    [No Abstract]   [Full Text] [Related]  

  • 31. [Hirschsprung-Galant infantilism].
    Fehlow P; Walther F
    Padiatr Grenzgeb; 1991; 30(3):245-52. PubMed ID: 2067874
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Rud's syndrome. Description of a case].
    Scribanis R; Buoncompagni A; Venzano V; Jamone R; Fasce L
    Minerva Pediatr; 1985 Oct; 37(20):823-6. PubMed ID: 4094600
    [No Abstract]   [Full Text] [Related]  

  • 33. Multicore disease in sibs with severe mental retardation, short stature, facial anomalies, hypoplasia of the pituitary fossa, and hypogonadotrophic hypogonadism.
    Chudley AE; Rozdilsky B; Houston CS; Becker LE; Knoll JH
    Am J Med Genet; 1985 Jan; 20(1):145-58. PubMed ID: 3970066
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Sjögren-Larsson syndrome].
    Vajda P; Brozmanová M; Szabová I
    Cesk Pediatr; 1982 Jun; 37(6):329-30. PubMed ID: 7105232
    [No Abstract]   [Full Text] [Related]  

  • 35. Sjögren-Larsson syndrome. Oligophrenia--ichthyosis--di-tetraplegia.
    Theile U
    Humangenetik; 1974 May; 22(2):91-118. PubMed ID: 4135782
    [No Abstract]   [Full Text] [Related]  

  • 36. Rud syndrome revisited: ichthyosis, mental retardation, epilepsy and hypogonadism.
    Marxmiller J; Trenkle I; Ashwal S
    Dev Med Child Neurol; 1985 Jun; 27(3):335-43. PubMed ID: 3926570
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The syndrome of Rud.
    MACGILLIVRAY RC
    Am J Ment Defic; 1954 Jul; 59(1):67-72. PubMed ID: 13158391
    [No Abstract]   [Full Text] [Related]  

  • 38. Dermatoglyphics in Börjeson-Forssman-Lehmann syndrome.
    Flannery DB; Piussan C; Wright LE
    Am J Med Genet; 1985 Jun; 21(2):401-4. PubMed ID: 4014320
    [No Abstract]   [Full Text] [Related]  

  • 39. [Primary hypogonadism associated with neuropsychiatric disorders].
    Fehlow P; Walther F
    Arztl Jugendkd; 1991; 82(2):93-102. PubMed ID: 1759640
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 46 3q+ karyotype presenting as syndrome with obesity and hypogonadism.
    Raman PG; Shende A; Chakraborty D; Akolekar SS
    J Assoc Physicians India; 2001 Apr; 49():481-4. PubMed ID: 11762626
    [No Abstract]   [Full Text] [Related]  

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