BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 2309763)

  • 1. Carpenter syndrome: marked variability of expression to include the Summitt and Goodman syndromes.
    Gershoni-Baruch R
    Am J Med Genet; 1990 Feb; 35(2):236-40. PubMed ID: 2309763
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Acrocephalopolysyndactyly type II--Carpenter syndrome: clinical spectrum and an attempt at unification with Goodman and Summit syndromes.
    Cohen DM; Green JG; Miller J; Gorlin RJ; Reed JA
    Am J Med Genet; 1987 Oct; 28(2):311-24. PubMed ID: 3322002
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial occurrence of Summitt syndrome or a variant example of Carpenter syndrome?
    Pierquin G; Seligmann R; Van Regemorter N
    Genet Couns; 1992; 3(2):101-5. PubMed ID: 1642806
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Syndromes 2. Pfeiffer syndrome].
    Freihofer HP
    Ned Tijdschr Tandheelkd; 1998 Jul; 105(7):245-6. PubMed ID: 11928428
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An etiologic and nosologic overview of craniosynostosis syndromes.
    Cohen MM
    Birth Defects Orig Artic Ser; 1975; 11(2):137-89. PubMed ID: 179637
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Normal intelligence in two children with Carpenter syndrome.
    Frias JL; Felman AH; Rosenbloom AL; Finkelstein SN; Hoyt WF; Hall BD
    Am J Med Genet; 1978; 2(2):191-9. PubMed ID: 263437
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Carpenter syndrome: natural history and clinical spectrum.
    Robinson LK; James HE; Mubarak SJ; Allen EJ; Jones KL
    Am J Med Genet; 1985 Mar; 20(3):461-9. PubMed ID: 3993675
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Carpenter syndrome with normal intelligence: Brazilian girl born to consanguineous parents.
    Richieri-Costa A; Pirolo Júnior L; Cohen MM
    Am J Med Genet; 1993 Aug; 47(2):281-3. PubMed ID: 8213921
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Intrafamilial variability of Pfeiffer-type cardiocranial syndrome.
    Digilio MC; Marino B; Borzaga U; Giannotti A; Dallapiccola B
    Am J Med Genet; 1997 Dec; 73(4):480-3. PubMed ID: 9415478
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Apert syndrome with partial preaxial polydactyly.
    Lefort G; Sarda P; Humeau C; Rieu D
    Genet Couns; 1992; 3(2):107-9. PubMed ID: 1642807
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Carpenter syndrome.
    Hidestrand P; Vasconez H; Cottrill C
    J Craniofac Surg; 2009 Jan; 20(1):254-6. PubMed ID: 19165041
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fontaine-Farriaux craniosynostosis: second report in the literature.
    Priolo M; De Toni T; Baffico M; Cama A; Seri M; Cusano R; Costabello L; Fondelli P; Capra V; Silengo M; Ravazzolo R; Lerone M
    Am J Med Genet; 2001 May; 100(3):214-8. PubMed ID: 11343306
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Apert's syndrome: (acrocephalosyndactylism).
    Meyer JL
    J Foot Surg; 1981; 20(4):210-13. PubMed ID: 6274945
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of Carpenter syndrome: looking beyond craniosynostosis and polysyndactyly.
    Victorine AS; Weida J; Hines KA; Robinson B; Torres-Martinez W; Weaver DD
    Am J Med Genet A; 2014 Mar; 164A(3):820-3. PubMed ID: 24458945
    [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. Cerebral malformations in Carpenter syndrome.
    Taravath S; Tonsgard JH
    Pediatr Neurol; 1993; 9(3):230-4. PubMed ID: 8352858
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Carpenter syndrome in a patient from Tanzania.
    Lodhia J; Rego-Garcia I; Koipapi S; Sadiq A; Msuya D; Spaendonk RV; Hamel B; Dekker M
    Am J Med Genet A; 2021 Mar; 185(3):986-989. PubMed ID: 33368989
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Apert syndrome in a newborn infant without craniosynostosis.
    Coomaralingam S; Roth P
    J Craniofac Surg; 2012 May; 23(3):e209-11. PubMed ID: 22627435
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal findings in carpenter syndrome and a novel mutation in RAB23.
    Haye D; Collet C; Sembely-Taveau C; Haddad G; Denis C; Soulé N; Suc AL; Listrat A; Toutain A
    Am J Med Genet A; 2014 Nov; 164A(11):2926-30. PubMed ID: 25168863
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.