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 *

131 related articles for article (PubMed ID: 30992743)

  • 1. Pfeiffer Syndrome with Extreme Proptosis, Hypothyroidism and Tail like Appendage.
    Soundaram V; ; Lewis LE; Girisha KM; Jayashree P; Balasubramanian S; Pratyusha R
    Oman Med J; 2014 Sep; 29(5):e080. PubMed ID: 30992743
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pfeiffer syndrome.
    Vogels A; Fryns JP
    Orphanet J Rare Dis; 2006 Jun; 1():19. PubMed ID: 16740155
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A case of Pfeiffer syndrome.
    Park MS; Yoo JE; Chung J; Yoon SH
    J Korean Med Sci; 2006 Apr; 21(2):374-8. PubMed ID: 16614535
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pfeiffer syndrome: a clinical review.
    Moore MH; Cantrell SB; Trott JA; David DJ
    Cleft Palate Craniofac J; 1995 Jan; 32(1):62-70. PubMed ID: 7727489
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ophthalmic considerations in patients with Pfeiffer syndrome.
    Clark JD; Compton CJ; Tahiri Y; Nunery WR; Harold Lee HB
    Am J Ophthalmol Case Rep; 2016 Jul; 2():1-3. PubMed ID: 29503887
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pfeiffer syndrome: systemic and ocular implications.
    Harb E; Kran B
    Optometry; 2005 Jul; 76(7):352-62. PubMed ID: 16038862
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Pfeiffer Syndrome type 2--case report.
    Oyamada MK; Ferreira HS; Hoff M
    Sao Paulo Med J; 2003 Jul; 121(4):176-9. PubMed ID: 14595512
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A case of Pfeiffer syndrome type 1 with an A344P mutation in the FGFR2 gene.
    Shotelersuk V; Srivuthana S; Ittiwut C; Theamboonlers A; Mahatumarat C; Poovorawan Y
    Southeast Asian J Trop Med Public Health; 2001 Jun; 32(2):425-8. PubMed ID: 11556600
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type III.
    Gripp KW; Stolle CA; McDonald-McGinn DM; Markowitz RI; Bartlett SP; Katowitz JA; Muenke M; Zackai EH
    Am J Med Genet; 1998 Jul; 78(4):356-60. PubMed ID: 9714439
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pfeiffer Syndrome Type 3 and Prune Belly Anomaly in a Female: Case Report and Review.
    Peña-Padilla C; Viramontes-Aguilar L; Tavares-Macías G; Bobadilla-Morales L; L Cunningham M; Park S; Zapata-Aldana E; Corona-Rivera JR
    Fetal Pediatr Pathol; 2019 Oct; 38(5):412-417. PubMed ID: 31002276
    [No Abstract]   [Full Text] [Related]  

  • 13. [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]  

  • 14. Intestinal malrotation in a patient with Pfeiffer syndrome type 2.
    Zarate YA; Putnam PE; Saal HM
    Cleft Palate Craniofac J; 2010 Nov; 47(6):638-41. PubMed ID: 20509766
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutation.
    Rossi M; Jones RL; Norbury G; Bloch-Zupan A; Winter RM
    Clin Dysmorphol; 2003 Oct; 12(4):269-74. PubMed ID: 14564217
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Craniofacial, limb, and abdominal anomalies in a distinct syndrome: relation to the spectrum of Pfeiffer syndrome type 3.
    Barone CM; Marion R; Shanske A; Argamaso RV; Shprintzen RJ
    Am J Med Genet; 1993 Mar; 45(6):745-50. PubMed ID: 8456855
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis.
    Cohen MM
    Am J Med Genet; 1993 Feb; 45(3):300-7. PubMed ID: 8434615
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of type 2 Pfeiffer syndrome.
    Bernstein PS; Gross SJ; Cohen DJ; Tiller GR; Shanske AL; Bombard AT; Marion RW
    Ultrasound Obstet Gynecol; 1996 Dec; 8(6):425-8. PubMed ID: 9014285
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.