BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

231 related articles for article (PubMed ID: 5551881)

  • 1. Pfeiffer syndrome. An unusual type of acrocephalosyndactyly with broad thumbs and great toes.
    Martsolf JT; Cracco JB; Carpenter GG; O'Hara AE
    Am J Dis Child; 1971 Mar; 121(3):257-62. PubMed ID: 5551881
    [No Abstract]   [Full Text] [Related]  

  • 2. Pfeiffer syndrome: an unusual type of acrocephalosyndactyl with broad thumbs and great toes.
    Cracco J; Martzolf J; Carpenter GG; Jackson L; O'Hara AE
    Neurology; 1970 Apr; 20(4):414. PubMed ID: 5535071
    [No Abstract]   [Full Text] [Related]  

  • 3. Familial acrocephalosyndactyly (Pfeiffer syndrome).
    Saldino RM; Steinbach HL; Epstein CJ
    Am J Roentgenol Radium Ther Nucl Med; 1972 Nov; 116(3):609-22. PubMed ID: 4641185
    [No Abstract]   [Full Text] [Related]  

  • 4. L--pfeiffer syndrome.
    Temptamy S; Safwat-Skoukry A; El-Meligy R
    Birth Defects Orig Artic Ser; 1974; 10(5):229-36. PubMed ID: 4469993
    [No Abstract]   [Full Text] [Related]  

  • 5. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
    Gnamey D; Farriaux JP
    J Genet Hum; 1971 Dec; 19(4):299-316. PubMed ID: 5152131
    [No Abstract]   [Full Text] [Related]  

  • 6. Apert's acrocephalosyndactyly in mother and daughter: cleft palate in the mother.
    Roberts KB; Hall JG
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):262-4. PubMed ID: 5173217
    [No Abstract]   [Full Text] [Related]  

  • 7. Pfeiffer syndrome: report of a family and review of the literature.
    Naveh Y; Friedman A
    J Med Genet; 1976 Aug; 13(4):277-80. PubMed ID: 957376
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [A case of Pfeiffer syndrome with psychomotor delay. Part I - Physical and X-ray examination and psychomotor assessment. Part II - Notes about surgical treatment of Pfeiffer syndrome and other craniofacial stenosis types].
    Ronconi GF; Pesenti P; Cenzi R; Baciliero U; Zanardo V; Curioni C
    Pediatr Med Chir; 1982; 4(4):459-66. PubMed ID: 7170223
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Anorectal anomaly in Pfeiffer syndrome.
    Ohashi H; Nishimoto H; Nishimura J; Sato M; Imaizumi S; Aihara T; Fukushima Y
    Clin Dysmorphol; 1993 Jan; 2(1):28-33. PubMed ID: 8298735
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pitfalls of genetic counselling in Pfeiffer's syndrome.
    Baraitser M; Bowen-Bravery M; Saldaña-Garcia P
    J Med Genet; 1980 Aug; 17(4):250-6. PubMed ID: 7205899
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Craniosynostosis, Philadelphia type: a new autosomal dominant syndrome with sagittal craniosynostosis and syndactyly of the fingers and toes.
    Robin NH; Segel B; Carpenter G; Muenke M
    Am J Med Genet; 1996 Mar; 62(2):184-91. PubMed ID: 8882401
    [TBL] [Abstract][Full Text] [Related]  

  • 12. On the classification of the acrocephalosyndactyly syndromes.
    Escobar V; Bixler D
    Clin Genet; 1977 Sep; 12(3):169-78. PubMed ID: 908170
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Are the acrocephalosyndactyly syndromes variable expressions of a single gene defect?
    Escobar V; Bixler D
    Birth Defects Orig Artic Ser; 1977; 13(3C):139-54. PubMed ID: 890108
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Broad thumbs and great toes syndrome. Rubinstein-Taybi syndrome.
    Bejar RL; Smith GF
    J Fla Med Assoc; 1969 Feb; 56(2):111-4. PubMed ID: 5773784
    [No Abstract]   [Full Text] [Related]  

  • 15. Triphalangeal thumb and brachy-ectrodactyly syndrome. Confirmation of autosomal dominant inheritance.
    Silengo MC; Biagioli M; Bell GL; Bona G; Franceschini P
    Clin Genet; 1987 Jan; 31(1):13-8. PubMed ID: 3568429
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Type V acrocephalosyndactylia (Pfeiffer's syndrome). Apropos of 3 cases in the same family].
    Manouvrier-Hanu S; Herbaux B; Pellerin P; Douchet P; Bouchez-Bonniere MC; Dubos JP; Farriaux JP
    Arch Fr Pediatr; 1989; 46(6):433-7. PubMed ID: 2783004
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [The Rubinstein-Taybi syndrome. Clinical and pneumoencephalographic findings].
    Neuhäuser G; Schulze H
    Z Kinderheilkd; 1968; 103(2):90-108. PubMed ID: 5303316
    [No Abstract]   [Full Text] [Related]  

  • 18. The Saethre-Chotzen syndrome with partial bifid of the distal phalanges of the great toes. Observations of three cases in one family.
    Kopyść Z; Stańska M; Ryzko J; Kulczyk B
    Hum Genet; 1980; 56(2):195-204. PubMed ID: 7450776
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Upper extremity anomalies in Pfeiffer syndrome and mutational correlations.
    Cerrato FE; Nuzzi LC; Theman TA; Taghinia A; Upton J; Labow BI
    Plast Reconstr Surg; 2014 May; 133(5):654e-661e. PubMed ID: 24776567
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial opposable triphalangeal thumbs associated with duplication of the big toes.
    Merlob P; Grunebaum M; Reisner SH
    J Med Genet; 1985 Feb; 22(1):78-80. PubMed ID: 3981586
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.