302 related articles for article (PubMed ID: 8882401)
21. A hereditable combination of congenital anomalies.
Agarwal RP; Jain D; Ramesh Babu CS; Garg RK
J Bone Joint Surg Br; 1996 May; 78(3):492-4. PubMed ID: 8636194
[TBL] [Abstract][Full Text] [Related]
22. A new case of Pfeiffer syndrome with mutation in FGFR2.
Addor MC; Gudinchet F; Laurini RN; Pescia G; Schorderet DF
Genet Couns; 1997; 8(4):303-9. PubMed ID: 9457499
[TBL] [Abstract][Full Text] [Related]
23. [Acrocephalosyndactyly I (Apert syndrome)].
Linss G
Hautarzt; 2000 Sep; 51(9):685-7. PubMed ID: 11057397
[TBL] [Abstract][Full Text] [Related]
24. Familial and hereditary anomalies producing brachydactylia of hands: roentgen manifestations.
Kellam DA
J Am Osteopath Assoc; 1970 Sep; 70(1):78-100. PubMed ID: 4990165
[No Abstract] [Full Text] [Related]
25. Pfeiffer syndrome.
Vogels A; Fryns JP
Orphanet J Rare Dis; 2006 Jun; 1():19. PubMed ID: 16740155
[TBL] [Abstract][Full Text] [Related]
26. Acrocephalopolysyndactyly, type Noack, in a large kindred.
Robinow M; Sorauf TJ
Birth Defects Orig Artic Ser; 1975; 11(5):99-106. PubMed ID: 1240778
[TBL] [Abstract][Full Text] [Related]
27. [Transverse extremity defects in a case of Adams-Oliver syndrome].
Fehlow P; Walther F
Padiatr Grenzgeb; 1990; 29(4):279-84. PubMed ID: 2216522
[TBL] [Abstract][Full Text] [Related]
28. [Apert's syndrome with polymetatarsia].
Nivelon A; Nivelon JL; Matthieu M; Piussan C; Maroteaux P
Ann Pediatr (Paris); 1991 Jan; 38(1):9-13. PubMed ID: 1848742
[TBL] [Abstract][Full Text] [Related]
29. Congenital stapes fixation, symphalangism and syndactylia.
Vase P; Prytz S; Pedersen PS
Acta Otolaryngol; 1975; 80(5-6):394-8. PubMed ID: 173134
[TBL] [Abstract][Full Text] [Related]
30. Craniosynostosis: Acrocephalosyndactyly (Apert Syndrome) Diagnosed in a Newborn.
Stomnaroska O; Danilovski D; Ivanovska S
Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2017 Dec; 38(3):153-155. PubMed ID: 29668474
[TBL] [Abstract][Full Text] [Related]
31. Auralcephalosyndactyly: a new craniosynostosis syndrome or a variant of the Saethre-Chotzen syndrome?
Legius E; Fryns JP; Van den Berghe H
J Med Genet; 1989 Aug; 26(8):522-4. PubMed ID: 2769726
[TBL] [Abstract][Full Text] [Related]
32. Ectrodactyly, ectodermal dysplasia and cleft lip syndrome.
Yap HK; Lee BW; Tay JS; Wong HB
J Singapore Paediatr Soc; 1985; 27(3-4):215-7. PubMed ID: 3831606
[No Abstract] [Full Text] [Related]
33. Family study of inherited syndrome with multiple congenital deformities: symphalangism, carpal and tarsal fusion, brachydactyly, craniosynostosis, strabismus, hip osteochondritis.
Ventruto V; Di Girlamo R; Festa B; Romano A; Sebastio G; Sebastio L
J Med Genet; 1976 Oct; 13(5):394-8. PubMed ID: 1003450
[TBL] [Abstract][Full Text] [Related]
34. Genetics and malformations of the hand.
Wynne-Davies R
Hand; 1971 Sep; 3(2):184-92. PubMed ID: 4331429
[No Abstract] [Full Text] [Related]
35. Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression?
Kwee ML; Lindhout D
Clin Genet; 1983 Sep; 24(3):200-5. PubMed ID: 6627724
[TBL] [Abstract][Full Text] [Related]
36. [Hereditary brachydactyly].
Rebollar Mesa JL
Rev Clin Esp; 1975 Jan; 136(2):169-72. PubMed ID: 1121594
[No Abstract] [Full Text] [Related]
37. Syndactyly of the ring and small finger.
De Smet L; Mulier T; Fabry G
Genet Couns; 1994; 5(1):45-9. PubMed ID: 8031535
[TBL] [Abstract][Full Text] [Related]
38. [Polydactyly].
Le Marec B; Bracq H; Lambotte C; Nivelon A; Pfeiffer R; Toudic L
J Genet Hum; 1982 Nov; 30(4):317-28. PubMed ID: 7169597
[TBL] [Abstract][Full Text] [Related]
39. [Hereditary brachydactyly with nail aplasia].
Santos HG; George FH; Ferreira JR
Acta Med Port; 1981; 3(2):147-60. PubMed ID: 7315521
[No Abstract] [Full Text] [Related]
40. Apparent Apert syndrome with polydactyly: rare pleiotropic manifestation or new syndrome?
Maroteaux P; Fonfria MC
Am J Med Genet; 1987 Sep; 28(1):153-8. PubMed ID: 3674108
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
