120 related articles for article (PubMed ID: 7253005)
21. Pfeiffer syndrome: analysis of a clinical series and development of a classification system.
Greig AV; Wagner J; Warren SM; Grayson B; McCarthy JG
J Craniofac Surg; 2013 Jan; 24(1):204-15. PubMed ID: 23348287
[TBL] [Abstract][Full Text] [Related]
22. [Syndromes 2. Pfeiffer syndrome].
Freihofer HP
Ned Tijdschr Tandheelkd; 1998 Jul; 105(7):245-6. PubMed ID: 11928428
[TBL] [Abstract][Full Text] [Related]
23. A family with the Saethre-Chotzen syndrome.
Bianchi E; Aricŏ M; Podestă AF; Grana M; Fiori P; Beluffi G
Am J Med Genet; 1985 Dec; 22(4):649-58. PubMed ID: 4073118
[TBL] [Abstract][Full Text] [Related]
24. Pfeiffer syndrome: oral healthcare management and description of new dental findings in a craniosynostosis.
Hassona Y; Al-Hadidi A; Ghlassi TA; Dali HE; Scully C
Spec Care Dentist; 2017 Sep; 37(5):258-262. PubMed ID: 28845899
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. 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]
27. Premature closure of the spheno-occipital synchondrosis in Pfeiffer syndrome: a link to midface hypoplasia.
Paliga JT; Goldstein JA; Vossough A; Bartlett SP; Taylor JA
J Craniofac Surg; 2014 Jan; 25(1):202-5. PubMed ID: 24406578
[TBL] [Abstract][Full Text] [Related]
28. Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation.
Chen CP; Lin SP; Su YN; Chien SC; Tsai FJ; Wang W
Genet Couns; 2008; 19(2):165-72. PubMed ID: 18618990
[TBL] [Abstract][Full Text] [Related]
29. [Acrocephalosyndactyly I (Apert syndrome)].
Linss G
Hautarzt; 2000 Sep; 51(9):685-7. PubMed ID: 11057397
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Negative autoregulation of fibroblast growth factor receptor 2 expression characterizing cranial development in cases of Apert (P253R mutation) and Pfeiffer (C278F mutation) syndromes and suggesting a basis for differences in their cranial phenotypes.
Britto JA; Moore RL; Evans RD; Hayward RD; Jones BM
J Neurosurg; 2001 Oct; 95(4):660-73. PubMed ID: 11596961
[TBL] [Abstract][Full Text] [Related]
32. [Acrocephalosyndactylia--Vogt syndrome].
Fehlow P; Walther F
Psychiatr Neurol Med Psychol (Leipz); 1985 Jun; 37(6):323-9. PubMed ID: 4034800
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Pfeiffer syndrome type 3, a rare and unusual craniosynostosis: case reports from Korle Bu Teaching Hospital, Accra, Ghana.
Badoe EV
West Afr J Med; 2013; 32(3):228-30. PubMed ID: 24122692
[TBL] [Abstract][Full Text] [Related]
35. Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses).
Kress W; Collmann H; Büsse M; Halliger-Keller B; Mueller CR
Cytogenet Cell Genet; 2000; 91(1-4):134-7. PubMed ID: 11173845
[TBL] [Abstract][Full Text] [Related]
36. Three-dimensional features of Pfeiffer syndrome.
Medina M; Cortés E; Eguiluz I; Barber MA
Int J Gynaecol Obstet; 2009 Jun; 105(3):266-7. PubMed ID: 19232609
[No Abstract] [Full Text] [Related]
37. Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review.
Nur BG; Pehlivanoğlu S; Mıhçı E; Calışkan M; Demir D; Alper OM; Kayserili H; Lüleci G
Pediatr Neurol; 2014 May; 50(5):482-90. PubMed ID: 24656465
[TBL] [Abstract][Full Text] [Related]
38. The Saethre-Chotzen syndrome.
Kreiborg S; Pruzansky S; Pashayan H
Teratology; 1972 Dec; 6(3):287-94. PubMed ID: 4643612
[No Abstract] [Full Text] [Related]
39. An unusual form of familial acrocephalosyndactyly.
Young ID; Harper PS
J Med Genet; 1982 Aug; 19(4):286-8. PubMed ID: 7120317
[TBL] [Abstract][Full Text] [Related]
40. [The problem of diagnosis and risk in cases of acrocephaly].
Predescu V; Christodorescu D
Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1975; 20(3):229-36. PubMed ID: 1085470
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]