78 related articles for article (PubMed ID: 2851938)
1. Recessive inheritance of apparent Apert syndrome with polysyndactyly?
Sidhu SS; Deshmukh R
Am J Med Genet; 1988 Sep; 31(1):179-80. PubMed ID: 2851938
[No Abstract] [Full Text] [Related]
2. Apert syndrome with polysyndactyly of the feet.
Gorlin RJ
Am J Med Genet; 1989 Apr; 32(4):557. PubMed ID: 2774006
[No Abstract] [Full Text] [Related]
3. Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 gene.
Mantilla-Capacho JM; Arnaud L; Díaz-Rodriguez M; Barros-Núñez P
Genet Couns; 2005; 16(4):403-6. PubMed ID: 16440883
[TBL] [Abstract][Full Text] [Related]
4. [Surgical treatment of hand syndactyly in Apert syndrome].
Guzanin S; Zábavníková M; Kacmár P; Sabovcík R; Kluka T
Acta Chir Orthop Traumatol Cech; 2001; 68(4):249-55. PubMed ID: 11706550
[TBL] [Abstract][Full Text] [Related]
5. Apparent autosomal recessive inheritance of the Treacher Collins syndrome.
Walker FA
Birth Defects Orig Artic Ser; 1974; 10(8):135-9. PubMed ID: 4376426
[No Abstract] [Full Text] [Related]
6. Apert syndrome.
Deshmukh LS; Rasheed SM
J Indian Med Assoc; 1996 Apr; 94(4):162. PubMed ID: 8854639
[No Abstract] [Full Text] [Related]
7. Syndactyly in Apert syndrome. Utility of a prognostic classification.
Journeau P; Lajeunie E; Rénier D; Salon A; Guéro S; Pouliquen JC
Ann Chir Main Memb Super; 1999; 18(1):13-9. PubMed ID: 10941391
[TBL] [Abstract][Full Text] [Related]
8. Syndactyly correction of the hand in Apert syndrome.
Zucker RM; Cleland HJ; Haswell T
Clin Plast Surg; 1991 Apr; 18(2):357-64. PubMed ID: 1648464
[TBL] [Abstract][Full Text] [Related]
9. Carpenter syndrome--acrocephalopolysyndactyly type II.
Eaton AP; Sommer A; Kontras SB; Sayers MP
Birth Defects Orig Artic Ser; 1974; 10(9):249-60. PubMed ID: 4370930
[No Abstract] [Full Text] [Related]
10. Depigmentation of hair, skin, and eyes associated with the Apert syndrome.
Margolis S; Siegel IM; Choy A; Breinin GM
Birth Defects Orig Artic Ser; 1978; 14(6B):341-60. PubMed ID: 728574
[No Abstract] [Full Text] [Related]
11. Mental retardation, hypotrichosis and syndactyly: a new entity?
Lopes VL; Marques-De-Faria AP
Genet Couns; 1996; 7(1):47-51. PubMed ID: 8652088
[TBL] [Abstract][Full Text] [Related]
12. Cenani-Lenz syndrome in father and daughter.
De Smet L; De Beer P; Fryns JP
Genet Couns; 1996; 7(2):153-7. PubMed ID: 8831136
[TBL] [Abstract][Full Text] [Related]
13. Filippi syndrome: report of three additional cases.
Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
[TBL] [Abstract][Full Text] [Related]
14. [Developmental disorders resembling Apert syndrome in a 2-year-old girl].
Karkowski MK
Pediatr Pol; 1989 May; 64(5):323-6. PubMed ID: 2560828
[No Abstract] [Full Text] [Related]
15. Apert syndrome.
Nicholas KC; Jorgenson RJ
Birth Defects Orig Artic Ser; 1975; 11(2):396. PubMed ID: 1227558
[No Abstract] [Full Text] [Related]
16. Dentofacial characteristics in Apert syndrome: a case report.
Batra P; Duggal R; Parkash H
J Indian Soc Pedod Prev Dent; 2002 Sep; 20(3):118-23. PubMed ID: 12435011
[TBL] [Abstract][Full Text] [Related]
17. [The Apert syndrome. Cytogenetic observations].
Gualandri V; Milesi M; Turuani E
Minerva Chir; 1966 Jul; 21(13):614-8. PubMed ID: 5968404
[No Abstract] [Full Text] [Related]
18. Pilosebaceous abnormalities in Apert type acrocephalosyndactyly.
Solomon LM; Cohen MM; Pruzansky S
Birth Defects Orig Artic Ser; 1971 Jun; 7(8):193-5. PubMed ID: 4281326
[TBL] [Abstract][Full Text] [Related]
19. Axillary osmidrosis in Apert syndrome: management with an arthroscopic shaver technique.
Hess J; Lonergan I; Rozzelle AA; Arneja JS
J Craniofac Surg; 2008 Jul; 19(4):1126-30. PubMed ID: 18650746
[TBL] [Abstract][Full Text] [Related]
20. Sliding hiatal hernia associated with Apert syndrome: a first case report.
Tastekin A; Kantarci M; Ors R; Ceviz N
Genet Couns; 2004; 15(3):387-9. PubMed ID: 15517835
[No Abstract] [Full Text] [Related]
[Next] [New Search]
