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 *

157 related articles for article (PubMed ID: 14187829)

  • 1. [LEPRECHAUNISM. (APROPOS OF A LITTLE KNOWN FORM OF FAMILIAL OLIGOPHRENIA)].
    BAMATTER F
    Rev Med Suisse Romande; 1964 Jun; 84():494-502. PubMed ID: 14187829
    [No Abstract]   [Full Text] [Related]  

  • 2. A NEWLY RECOGNIZED SYNDROME OF MULTIPLE CONGENITAL ANOMALIES.
    SMITH DW; LEMLI L; OPITZ JM
    J Pediatr; 1964 Feb; 64():210-7. PubMed ID: 14119520
    [No Abstract]   [Full Text] [Related]  

  • 3. ACANTHOSIS NIGRICANS AND CONGENITAL TOTAL LIPODYSTROPHY: ASSOCIATED ANOMALIES OBSERVED IN TWO SIBLINGS.
    BRUBAKER MM; LEVAN NE; COLLIPP PJ
    Arch Dermatol; 1965 Apr; 91():320-5. PubMed ID: 14275493
    [No Abstract]   [Full Text] [Related]  

  • 4. CONGENITAL LIPODYSTROPHIC DIABETES WITH ACANTHOSIS NIGRICANS: THE SEIP-LAWRENCE SYNDROME.
    REED WB; DEXTER R; CORLEY C; FISH C
    Arch Dermatol; 1965 Apr; 91():326-34. PubMed ID: 14275494
    [No Abstract]   [Full Text] [Related]  

  • 5. Leprechaunism (Donohue syndrome).
    Gross-Kieselstein E; Ben-Galim E; Amir N; Abrahamov A
    Am J Dis Child; 1973 Oct; 126(4):500-3. PubMed ID: 4131563
    [No Abstract]   [Full Text] [Related]  

  • 6. DYSTROPHIC CHANGES ASSOCIATED WITH LEPRECHAUNISM IN A MALE INFANT.
    SALMON MA; WEBB JN
    Arch Dis Child; 1963 Oct; 38(201):530-5. PubMed ID: 14065999
    [No Abstract]   [Full Text] [Related]  

  • 7. LEPRECHAUNISM (DONOHUE'S SYNDROME).
    KALLO A; LAKATOS I; SZIJARTO L
    J Pediatr; 1965 Feb; 66():372-9. PubMed ID: 14258927
    [No Abstract]   [Full Text] [Related]  

  • 8. THE BOERJESON-FORSSMAN-LEHMANN SYNDROME.
    BAAR HS; GALINDO J
    J Ment Defic Res; 1965 Jun; 9():125-30. PubMed ID: 14323171
    [No Abstract]   [Full Text] [Related]  

  • 9. THE FUTURE OF THE HEALTH DEPARTMENT IN MEDICAL GENETICS.
    ANDERSON UM; BANNERMAN RM
    Am J Public Health Nations Health; 1965 Jun; 55(6):866-72. PubMed ID: 14295910
    [No Abstract]   [Full Text] [Related]  

  • 10. [GENETIC MENTAL DEFICIENCY].
    NODOT A
    Rev Neuropsychiatr Infant; 1963; 11():433-46. PubMed ID: 14200146
    [No Abstract]   [Full Text] [Related]  

  • 11. [Humoral and cellular immunity in children with Donohue's syndrome (leprechaunism)].
    Dyduch A; Karczewska K; Bubała H; Kasner J; Lukas A; Lukasik M; Szczepański Z; Rokicka B
    Pediatr Pol; 1982; 57(9):739-42. PubMed ID: 6984895
    [No Abstract]   [Full Text] [Related]  

  • 12. HOMOCYSTINURIA: CLINICAL AND PATHOLOGICAL REVIEW OF TEN CASES.
    CARSON NA; DENT CE; FIELD CM; GAULL GE
    J Pediatr; 1965 Mar; 66():565-83. PubMed ID: 14264314
    [No Abstract]   [Full Text] [Related]  

  • 13. FAMILIAL HYPERPROLINEMIA. REPORT OF A SECOND CASE, ASSOCIATED WITH CONGENITAL RENAL MALFORMATIONS, HEREDITARY HEMATURIA AND MILD MENTAL RETARDATION, WITH DEMONSTRATION OF AN ENZYME DEFECT.
    EFRON ML
    N Engl J Med; 1965 Jun; 272():1243-54. PubMed ID: 14290545
    [No Abstract]   [Full Text] [Related]  

  • 14. Integration of human genetic studies in clinical medicine.
    Veale AM
    J R Coll Physicians Lond; 1971 Oct; 6(1):41-52. PubMed ID: 5166661
    [No Abstract]   [Full Text] [Related]  

  • 15. Donohue's syndrome--leprechaunism--Cockayne's syndrome. A report of two patients and discussion of the relation between Donohue's Syndrome and Cockayne's Syndrome.
    Gamstorp I
    Eur Neurol; 1972; 7(1):26-33. PubMed ID: 5019154
    [No Abstract]   [Full Text] [Related]  

  • 16. Metaphyseal and epiphyseal dysplasia with unusual facies and cataract.
    Kozlowski K; Rafinski T; Kucharska K
    Am J Dis Child; 1973 Apr; 125(4):553-6. PubMed ID: 4699894
    [No Abstract]   [Full Text] [Related]  

  • 17. BRACHYDACTYLY, PECULIAR FACIES AND MENTAL RETARDATION.
    COFFIN GS
    Am J Dis Child; 1964 Oct; 108():351-9. PubMed ID: 14186654
    [No Abstract]   [Full Text] [Related]  

  • 18. [POLYDYSTROPHIC OLIGOPHRENIA (HEPARIN-SULFATE TYPE MUCOPOLYSACCHARIDOSIS)].
    MAROTEAUX P; LAMY M
    Presse Med (1893); 1964 Nov; 72():2991-6. PubMed ID: 14218742
    [No Abstract]   [Full Text] [Related]  

  • 19. Bird-beaded dwarfs (Seckel's syndrome). A familial pattern of developmental, dental, skeletal, genital, and central nervous system anomalies.
    Harper RG; Orti E; Baker RK
    J Pediatr; 1967 May; 70(5):799-804. PubMed ID: 6022184
    [No Abstract]   [Full Text] [Related]  

  • 20. SEQUELAE OF INFANTILE HYPERCALCAEMIA.
    JOSEPH MC
    Dev Med Child Neurol; 1964 Aug; 6():419-21. PubMed ID: 14210672
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.