132 related articles for article (PubMed ID: 957376)
1. 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]
2. 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]
3. [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]
4. 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]
5. Ruvalcaba syndrome: autosomal dominant inheritance.
Sugio Y; Kajii T
Am J Med Genet; 1984 Dec; 19(4):741-53. PubMed ID: 6517098
[TBL] [Abstract][Full Text] [Related]
6. Saethre-Chotzen syndrome: a broad and variable pattern of skeletal malformations.
Friedman JM; Hanson JW; Graham CB; Smith DW
J Pediatr; 1977 Dec; 91(6):929-23. PubMed ID: 925822
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Pfeiffer syndrome.
Vogels A; Fryns JP
Orphanet J Rare Dis; 2006 Jun; 1():19. PubMed ID: 16740155
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. [Feingold syndrome].
Alessandri JL; Graber D; Tiran-Rajaofera I; Montbrun A; Pilorget H; Samperiz S; Attali T; de Napoli-Cocci S
Arch Pediatr; 2000 Jun; 7(6):637-40. PubMed ID: 10911531
[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. 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]
13. The Summitt syndrome: observations on a third case.
Sells CJ; Hanson JW; Hall JG
Am J Med Genet; 1979; 3(1):27-33. PubMed ID: 474616
[TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies.
Innis JW; Asher JH; Poznanski AK; Sheldon S
Am J Med Genet; 1997 Aug; 71(2):150-5. PubMed ID: 9217213
[TBL] [Abstract][Full Text] [Related]
15. Limb pterygium syndromes: a review and report of eleven patients.
Hall JG; Reed SD; Rosenbaum KN; Gershanik J; Chen H; Wilson KM
Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793
[TBL] [Abstract][Full Text] [Related]
16. Dominant inheritance of a syndrome similar to Rubinstein-Taybi.
Cotsirilos P; Taylor JC; Matalon R
Am J Med Genet; 1987 Jan; 26(1):85-93. PubMed ID: 3812583
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]