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 *

120 related articles for article (PubMed ID: 7253005)

  • 41. 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]  

  • 42. [Pfeiffer syndrome associated with clover-leaf skull: 1st case described in Venezuela].
    Martínez-Basalo C; Alvarez-Nava F; González-Inciarte ME; González-Inciarte L; Delgado-Luengo W; Mora-La Cruz E; Peña J; Rodríguez B; Gómez-Polo G; Delgado-Luengo J
    Invest Clin; 1997 Jun; 38(2):95-106. PubMed ID: 9296644
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Apert syndrome.
    Suparta N; Hartono ; Sunartini
    Paediatr Indones; 1991; 31(11-12):319-24. PubMed ID: 1845657
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. Pfeiffer syndrome: the importance of prenatal diagnosis.
    Nieuwenhuyzen-De Boer GM; Hoogeboom AJ; Smit LS; Heydanus R; Eggink AJ
    Eur J Obstet Gynecol Reprod Biol; 2014 Oct; 181():339-40. PubMed ID: 25183684
    [No Abstract]   [Full Text] [Related]  

  • 46. Pfeiffer syndrome: literature review of prenatal sonographic findings and genetic diagnosis.
    Giancotti A; D'Ambrosio V; Marchionni E; Squarcella A; Aliberti C; La Torre R; Manganaro L; Pizzuti A;
    J Matern Fetal Neonatal Med; 2017 Sep; 30(18):2225-2231. PubMed ID: 27762162
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.
    Rutland P; Pulleyn LJ; Reardon W; Baraitser M; Hayward R; Jones B; Malcolm S; Winter RM; Oldridge M; Slaney SF
    Nat Genet; 1995 Feb; 9(2):173-6. PubMed ID: 7719345
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Pfeiffer syndrome type 3 with FGR2 c.1052C>G (p.Ser351Cys) variant in West Africa: a case report.
    Danso KA; Akuaku RS; Young FNA; Wiafe SA
    Pan Afr Med J; 2021; 40():136. PubMed ID: 34909104
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Familial acrocephalosyndactylia with features of the Saethre-Chotzen syndrome].
    Kopyść Z; Kulczyk B; Ryzko J; Gura C; Stańska M; Kowalski K
    Pediatr Pol; 1979 Jul; 54(7):769-72. PubMed ID: 530768
    [No Abstract]   [Full Text] [Related]  

  • 50. Prenatal ultrasound diagnosis of a case of Pfeiffer syndrome without cloverleaf skull and review of the literature.
    Nazzaro A; Della Monica M; Lonardo F; Di Blasi A; Baffico M; Baldi M; Nazzaro G; De Placido G; Scarano G
    Prenat Diagn; 2004 Nov; 24(11):918-22. PubMed ID: 15565658
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [A study of genetic heterogeneity in Pfeiffer syndrome].
    Ma H; Wang Y; Mi Z; Hao M; Yang L; Zhao S; Ji S; Jing Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Apr; 15(2):81-4. PubMed ID: 9531645
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [Pfeiffer syndrome : a peculiar type of acrocephalosyndactyly (author's transl)].
    Plenier V; Resche F; Delaire J
    Rev Stomatol Chir Maxillofac; 1981; 82(4):251-7. PubMed ID: 6944761
    [No Abstract]   [Full Text] [Related]  

  • 53. Prenatal fetoscopic diagnosis of the Apert syndrome.
    Leonard CO; Daikoku NH; Winn K
    Am J Med Genet; 1982 Jan; 11(1):5-9. PubMed ID: 7065003
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Pfeiffer syndrome or Saethre-Chotzen syndrome?
    Tsukahara M; Hagiwara K; Kajii T
    Jinrui Idengaku Zasshi; 1985 Jun; 30(2):51-6. PubMed ID: 4087491
    [No Abstract]   [Full Text] [Related]  

  • 55. Pfeiffer's type of acrocephalosyndactyly in two families.
    Vanĕk J; Losan F
    J Med Genet; 1982 Aug; 19(4):289-92. PubMed ID: 7120318
    [TBL] [Abstract][Full Text] [Related]  

  • 56. A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome.
    de Ravel TJ; Taylor IB; Van Oostveldt AJ; Fryns JP; Wilkie AO
    Eur J Hum Genet; 2005 Apr; 13(4):503-5. PubMed ID: 15523492
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia.
    Chen CP; Lin SP; Liu YP; Chern SR; Chen SW; Lai ST; Wang W
    Taiwan J Obstet Gynecol; 2017 Jun; 56(3):412-414. PubMed ID: 28600064
    [No Abstract]   [Full Text] [Related]  

  • 59. Pfeiffer's syndrome family tree. Review of the literature.
    Lyon JR; Burgess RC
    Clin Orthop Relat Res; 1993 Sep; (294):294-8. PubMed ID: 8358932
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A severe case of Pfeiffer syndrome associated with stub thumb on the maternal side of the family.
    Kreiborg S; Cohen MM
    J Craniofac Genet Dev Biol; 1993; 13(2):73-5. PubMed ID: 8325969
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.