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: 967566)

  • 1. Symphalangism with metacarpophalangeal fusions and elbow abnormalities.
    Kassner EG; Katz I; Qazi QH
    Pediatr Radiol; 1976 Feb; 4(2):103-7. PubMed ID: 967566
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nievergelt-Pearlman syndrome with impairment of hearing. Report of three cases in a family.
    Murakami Y
    J Bone Joint Surg Br; 1975 Aug; 57(3):367-72. PubMed ID: 1158949
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The multiple synostoses syndrome. A plea for simplicity.
    Nixon JR
    Clin Orthop Relat Res; 1978 Sep; (135):48-51. PubMed ID: 709952
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tarsal and carpal coalition and symphalangism of the Fuhrmann type. Report of a family.
    Drawbert JP; Stevens DB; Cadle RG; Hall BD
    J Bone Joint Surg Am; 1985 Jul; 67(6):884-9. PubMed ID: 4019538
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mesomelic dysplasia with absence of fibulae and hexadactyly: Nievergelt syndrome or new syndrome?
    Petrella R; Ludman MD; Rabinowitz JG; Gilbert F; Hirschhorn K
    Am J Med Genet; 1990 Sep; 37(1):10-4. PubMed ID: 2240023
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nievergelt-Pearlman syndrome. Synostosis in feet and hands with dysplasia of elbows. Report of a case.
    Dubois HJ
    J Bone Joint Surg Br; 1970 May; 52(2):325-9. PubMed ID: 5445413
    [No Abstract]   [Full Text] [Related]  

  • 7. Symphalangism and brachydactyly syndrome: report of the WL symphalangism-brachydactyly syndrome: review of literature and classification.
    Herrmann J
    Birth Defects Orig Artic Ser; 1974; 10(5):23-53. PubMed ID: 4469994
    [No Abstract]   [Full Text] [Related]  

  • 8. Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome.
    Takahashi T; Takahashi I; Komatsu M; Sawaishi Y; Higashi K; Nishimura G; Saito H; Takada G
    Clin Genet; 2001 Dec; 60(6):447-51. PubMed ID: 11846737
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Family study of inherited syndrome with multiple congenital deformities: symphalangism, carpal and tarsal fusion, brachydactyly, craniosynostosis, strabismus, hip osteochondritis.
    Ventruto V; Di Girlamo R; Festa B; Romano A; Sebastio G; Sebastio L
    J Med Genet; 1976 Oct; 13(5):394-8. PubMed ID: 1003450
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [High-grade numerical plus variant of the hand and foot].
    Schenk R; Jacquemain B
    Z Orthop Ihre Grenzgeb; 1969 Jan; 105(4):515-27. PubMed ID: 4240747
    [No Abstract]   [Full Text] [Related]  

  • 12. Proximal symphalangism of fingers associated with fusion of os naviculare and talus and occurrence of two accessory bones in the feet (os paranaviculare and os tibiale externum) in an European--Indonesian--Chinese family.
    Wildervanck LS; Goedhard G; Meijer S
    Acta Genet Stat Med; 1967; 17(1):166-77. PubMed ID: 5633139
    [No Abstract]   [Full Text] [Related]  

  • 13. Nievergelt syndrome (mesomelic dwarfism-type Nievergelt).
    Young LW; Wood BP
    Birth Defects Orig Artic Ser; 1974; 10(5):81-6. PubMed ID: 4469999
    [No Abstract]   [Full Text] [Related]  

  • 14. A pedigree with unusual anomalies of the elbows, wrists and hands in five generations.
    Liebenberg F
    S Afr Med J; 1973 May; 47(17):745-8. PubMed ID: 4702300
    [No Abstract]   [Full Text] [Related]  

  • 15. Camptobrachydactyly: a new autosomal dominant trait with two probable homozygotes.
    Edwards JA; Gale RP
    Am J Hum Genet; 1972 Jul; 24(4):464-74. PubMed ID: 5031984
    [No Abstract]   [Full Text] [Related]  

  • 16. Patient with the mesomelic dysplasia, Nievergelt syndrome, and cerebellovermian agenesis and cataracts.
    Tüysüz B; Zeybek C; Zorer G; Sipahi O; Ungür S
    Am J Med Genet; 2002 May; 109(3):206-10. PubMed ID: 11977180
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Associated malformations of the head and extremities].
    Tridon P
    J Genet Hum; 1974 Dec; 22(4):365-80. PubMed ID: 4282383
    [No Abstract]   [Full Text] [Related]  

  • 18. FAMILIAL TARSAL AND CARPAL SYNOSTOSIS WITH RADIAL-HEAD SUBLUXATION (NIEVERGELT'S SYNDROME).
    PEARLMAN HS; EDKIN RE; WARREN RF
    J Bone Joint Surg Am; 1964 Apr; 46():585-92. PubMed ID: 14133342
    [No Abstract]   [Full Text] [Related]  

  • 19. [Multiple synostosis].
    Czeizel E; Göblyös P
    Orv Hetil; 1993 Aug; 134(35):1917-20. PubMed ID: 8395675
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial symphalangism syndrome transmitted through five generations.
    Moumoumi H; Mayelo V; Anthonioz P
    Genet Couns; 1991; 2(3):139-46. PubMed ID: 1801849
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.