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 *

91 related articles for article (PubMed ID: 4092386)

  • 1. [Indifference to pain with partial hemihypertrophy and spontaneous deep pain].
    Ishiai S; Kobayashi T; Furukawa T; Tsukagoshi H; Takai S
    Rinsho Shinkeigaku; 1985 Oct; 25(10):1126-30. PubMed ID: 4092386
    [No Abstract]   [Full Text] [Related]  

  • 2. [Growth disorders. Classification, diagnosis, therapy. 3. Excessive growth: constitutional tallness, endocrine tallness, chromosome abnormalities, tallness with unusual proportions, tallness in metabolic diseases].
    Butenandt O
    Fortschr Med; 1979 Nov; 97(44):2034-5. PubMed ID: 511085
    [No Abstract]   [Full Text] [Related]  

  • 3. Congenital sensory neuropathy in siblings.
    Haddow JE; Shapiro SR; Gall DG
    Pediatrics; 1970 Apr; 45(4):651-5. PubMed ID: 4191331
    [No Abstract]   [Full Text] [Related]  

  • 4. [The current status of medical genetics and its significance in neuropathology and psychiatry].
    Davidenkova EF
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1966; 66(11):1601-8. PubMed ID: 4234111
    [No Abstract]   [Full Text] [Related]  

  • 5. Amniocentesis for prenatal genetic studies.
    Milunsky A; Atkins L; Littlefield JW
    Obstet Gynecol; 1972 Jul; 40(1):104-8. PubMed ID: 4261531
    [No Abstract]   [Full Text] [Related]  

  • 6. The molecular genetics of neurological disease. Recent advances.
    Rosenberg RN
    Neurologia; 1993 May; 8(5):116-23. PubMed ID: 8507504
    [No Abstract]   [Full Text] [Related]  

  • 7. [Genetics and medicine].
    Efroimson VP
    Klin Med (Mosk); 1974 Jun; 52(6):11-8. PubMed ID: 4608120
    [No Abstract]   [Full Text] [Related]  

  • 8. Diagnosis of a triploid fetus at genetic amniocentesis.
    Porreco RP; Matson MR; Young PE; Bradshaw C; Leopold G; Jones OW
    Obstet Gynecol; 1980 Jul; 56(1):115-8. PubMed ID: 7383475
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Identification of the small submetacentric supernumerary chromosome in the cat's-eye syndrome].
    Noël B; Mottet J; Nantois Y; Quack B
    J Genet Hum; 1973 Mar; 21(1):23-32. PubMed ID: 4742121
    [No Abstract]   [Full Text] [Related]  

  • 10. [Sex chromatin corpuscle in psychiatry].
    Gini R; Caldararo JC; Pérez Arancibia L
    Prensa Med Argent; 1970 Mar; 57(2):64-7. PubMed ID: 5453138
    [No Abstract]   [Full Text] [Related]  

  • 11. [Monogenic inheritance: nervous system and neuromuscular diseases].
    Moser H
    Ther Umsch; 1986 Dec; 43(12):893-906. PubMed ID: 3824260
    [No Abstract]   [Full Text] [Related]  

  • 12. [Chromosome instability in diseases of the nervous system].
    Malygina NA; Badalian LO; Khandogina EK; Mutovin GR; Kalinina LV
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1987; 87(3):366-70. PubMed ID: 3554858
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Trisomy of group C (47, XX, C+)].
    Emberger JM; Rey J; Rieu D; Dossa D; Bonnet H; Jean R
    Arch Fr Pediatr; 1970; 27(10):1081-8. PubMed ID: 5495708
    [No Abstract]   [Full Text] [Related]  

  • 14. [Genetic problems in neurologic diseases--consulting aspects].
    Berg K
    Nord Med; 1971 May; 85(21):670-1. PubMed ID: 5581420
    [No Abstract]   [Full Text] [Related]  

  • 15. [Genetics of neuropsychiatric disorders].
    Cacabelos R
    Med Clin (Barc); 1990 May; 94(18):699-701. PubMed ID: 2388495
    [No Abstract]   [Full Text] [Related]  

  • 16. [Problems in practical medical genetics].
    Fradin ; Girard ; Jeune ; Paufique ; Robert
    Lyon Med; 1969 Jul; 222(27):11-41. PubMed ID: 4249539
    [No Abstract]   [Full Text] [Related]  

  • 17. [Triplet expansion diseases].
    Sablonnière B; Vuillaume I; Schraen-Maschke S
    Ann Biol Clin (Paris); 2000; 58(3):356-60. PubMed ID: 10846241
    [No Abstract]   [Full Text] [Related]  

  • 18. Short stature and language delay in a 5-year-old girl: 18p- syndrome.
    Grush ML; Kimberling WJ; Lynch HT
    Nebr Med J; 1982 Sep; 67(9):261-3. PubMed ID: 7133223
    [No Abstract]   [Full Text] [Related]  

  • 19. Ring chromosome 15 syndrome.
    Fryns JP; Jaeken J; Devlieger H; Debucquoy P; Eggermont E; Van den Berghe H
    Acta Paediatr Belg; 1981; 34(1):47-9. PubMed ID: 7270144
    [No Abstract]   [Full Text] [Related]  

  • 20. The syndrome of ring chromosome 12.
    Scribanu N; McCullars EB; Baumiller RC; Colon AR
    Am J Med Genet; 1980; 5(2):165-70. PubMed ID: 7395909
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.