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 *

160 related articles for article (PubMed ID: 6642505)

  • 1. Incidence at birth of different types of limb reduction abnormalities in Hungary 1975-1977.
    Bod M; Czeizel A; Lenz W
    Hum Genet; 1983; 65(1):27-33. PubMed ID: 6642505
    [TBL] [Abstract][Full Text] [Related]  

  • 2. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L; Corsello G; Giuffrè M; Piccione M; Albanese A
    Am J Med Genet; 1994 Jul; 51(3):266-9. PubMed ID: 8074157
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorder.
    Kantaputra PN; Gorlin RJ; Langer LO
    Am J Med Genet; 1992 Dec; 44(6):730-7. PubMed ID: 1481840
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Characteristics of certain types of limb reduction abnormalities].
    Bod M; Czeizel E; Lenz W
    Orv Hetil; 1985 Aug; 126(31):1917-20. PubMed ID: 4034183
    [No Abstract]   [Full Text] [Related]  

  • 5. [Congenital radioulnar synostosis].
    PALMA RODRIGUEZ A; BALEN BEJARANO E
    Rev Clin Esp; 1956 Apr; 61(1):44-6. PubMed ID: 13350755
    [No Abstract]   [Full Text] [Related]  

  • 6. [A case of congenital bilateral radio-ulnar synostosis].
    EXPOSITO L; GOMEZ DE ROSAS N
    Rev Cubana Pediatr; 1953 Mar; 25(3):171-3. PubMed ID: 13074927
    [No Abstract]   [Full Text] [Related]  

  • 7. Family study of congenital limb reduction abnormalities in Hungary 1975-1977.
    Czeizel A; Bod M; Lenz W
    Hum Genet; 1983; 65(1):34-45. PubMed ID: 6642506
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [On a case of congenital radio-ulnar synostosis treated surgically].
    CALABRO F
    Arch Ortop; 1959; 72():1246-53. PubMed ID: 13806850
    [No Abstract]   [Full Text] [Related]  

  • 9. Reconstructive surgery of major congenital skeletal deformities of the limbs.
    Sharrard WJ
    Dev Med Child Neurol; 1969 Apr; 11(2):153-61. PubMed ID: 5787714
    [No Abstract]   [Full Text] [Related]  

  • 10. Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1.
    Debeer P; Vandenbossche L; de Ravel TJ; Desloovere C; De Smet L; Huysmans C; Thoelen R; Vermeesch J; Van de Ven WJ; Fryns JP
    Clin Genet; 2004 Feb; 65(2):153-5. PubMed ID: 14984476
    [No Abstract]   [Full Text] [Related]  

  • 11. [Luxation, congenital radio-ulnar synostosis and dysplasia of the prono-supinator complexus; study of 3 familial cases and attempted classification of the congenital deformities of the elbow region].
    CAPECCHI V; CASINI E
    Arch Ortop; 1955; 68(1):24-49. PubMed ID: 14389036
    [No Abstract]   [Full Text] [Related]  

  • 12. Limb deficiency syndrome in half-sibs.
    Hecht JT; Scott CI
    Clin Genet; 1981 Dec; 20(6):432-7. PubMed ID: 7337959
    [No Abstract]   [Full Text] [Related]  

  • 13. [Malformation-retardation syndrome with bilateral absence of the 5th rays in both hands and feets, cleft palate, malformed ears and eyelids, radioulnar synostosis (author's transl)].
    Wiedemann HR
    Klin Padiatr; 1973 May; 185(3):181-6. PubMed ID: 4795571
    [No Abstract]   [Full Text] [Related]  

  • 14. [Genetic counseling in defect abnormalities of the extremities (proceedings)].
    Lenz W
    Z Orthop Ihre Grenzgeb; 1978 Aug; 116(4):558-60. PubMed ID: 212892
    [No Abstract]   [Full Text] [Related]  

  • 15. Causal study of isolated ulnar-fibular deficiency in Hungary, 1975-1984.
    Czeizel AE; Vitéz M; Kodaj I; Lenz W
    Am J Med Genet; 1993 Jun; 46(4):427-33. PubMed ID: 8357016
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Fibulo-ulnar hypoplasia with spherical ankle joint, radiation defects and synostoses].
    Henssge J; Engelke B
    Z Orthop Ihre Grenzgeb; 1970 Mar; 107(3):502-16. PubMed ID: 4245894
    [No Abstract]   [Full Text] [Related]  

  • 17. Hypoplasia/aplasia of pelvis, femora, fibulae, ulna, digits and nails: Fuhrmann syndrome without WNT7A mutations.
    Girisha KM; Vasudevan TG; Saadi AV; Shah H; Gopinath PM; Satyamoorthy K
    Clin Dysmorphol; 2011 Oct; 20(4):205-209. PubMed ID: 21716096
    [No Abstract]   [Full Text] [Related]  

  • 18. Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defects.
    Turnpenny PD; Dean JC; Duffty P; Reid JA; Carter P
    J Med Genet; 1992 Sep; 29(9):659-62. PubMed ID: 1404297
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary ulnar and fibular dimelia with peculiar facies. A case report.
    Sandrow RE; Sullivan PD; Steel HH
    J Bone Joint Surg Am; 1970 Mar; 52(2):367-70. PubMed ID: 4314818
    [No Abstract]   [Full Text] [Related]  

  • 20. Humero-radial synostosis with ulnar defects in sibs.
    Ramer JC; Ladda RL
    Am J Med Genet; 1989 Jun; 33(2):176-9. PubMed ID: 2669480
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.