139 related articles for article (PubMed ID: 7169597)
1. [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]
2. [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]
3. [Hand and foot deformities in a type I trichorhinophalangeal syndrome. Studies in 3 members of a family].
Meyer HH; Prescher W; Reime J
Z Orthop Ihre Grenzgeb; 1988; 126(1):34-8. PubMed ID: 3381568
[TBL] [Abstract][Full Text] [Related]
4. A syndrome of polydactyly-syndactyly and triphalangeal thumbs in three generations.
Yujnovsky O; Ayala D; Vincitorio A; Viale H; Sakati N; Nyhan WL
Clin Genet; 1974; 6(1):51-9. PubMed ID: 4372010
[No Abstract] [Full Text] [Related]
5. [Stapes ankylosis as a symptom of autosomal dominant symphalangia].
Theunissen EJ; Cremers CW
Ned Tijdschr Geneeskd; 1984 Apr; 128(15):712-4. PubMed ID: 6717641
[No Abstract] [Full Text] [Related]
6. [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]
7. Bilateral preaxial polydactyly: a possible dominant inheritant.
Nishikawa M; Bitoh N; Kikkawa F; Horii E; Mizutani S
Arch Gynecol Obstet; 2003 Oct; 268(4):337-9. PubMed ID: 14504883
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
Henkel KE; Pfeiffer RA; Stöss H
Pathologe; 1993 Mar; 14(2):91-2. PubMed ID: 8469651
[No Abstract] [Full Text] [Related]
10. The extra digit. A pointer to the eye?
Calver D; Keast-Butler J; Taylor D
Trans Ophthalmol Soc U K (1962); 1981; 101(1):35-8. PubMed ID: 6821009
[TBL] [Abstract][Full Text] [Related]
11. Crossed polydactyly type I in a mother and son: an autosomal dominant trait?
Ishikiriyama S; Sawada H; Nambu H; Niikawa N
Am J Med Genet; 1991 Jul; 40(1):41-3. PubMed ID: 1887848
[TBL] [Abstract][Full Text] [Related]
12. Distal obstructive uropathy with polydactyly: a new syndrome?
Halal F
Am J Med Genet; 1986 Aug; 24(4):753-7. PubMed ID: 3740105
[No Abstract] [Full Text] [Related]
13. [The Coffin-Siris syndrome. Case report].
Giovannucci Uzielli ML; Seminara S; Nicòtina PA; Consumi I; La Cauza C
Minerva Pediatr; 1980 Feb; 32(4):245-54. PubMed ID: 6770244
[No Abstract] [Full Text] [Related]
14. Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.
Guttmacher AE
Am J Med Genet; 1993 Apr; 46(2):219-22. PubMed ID: 8484413
[TBL] [Abstract][Full Text] [Related]
15. Crossed polydactyly.
Hosalkar HS; Shah H; Gujar P; Kulkarni AD
J Postgrad Med; 1999; 45(3):90-2. PubMed ID: 10734344
[TBL] [Abstract][Full Text] [Related]
16. The study of genetic variation in Nigeria. II. The genetics of polydactyly.
Scott-Emuakpor AB; Madueke ED
Hum Hered; 1976; 26(3):198-202. PubMed ID: 955643
[TBL] [Abstract][Full Text] [Related]
17. Tibial aplasia-ectrodactyly as variant expression of the Gollop-Wolfgang complex: report of a Brazilian family.
Richieri-Costa A; Brunoni D; Laredo Filho J; Kasinski S
Am J Med Genet; 1987 Dec; 28(4):971-80. PubMed ID: 3688036
[TBL] [Abstract][Full Text] [Related]
18. Relatively high prevalence of the Meckel syndrome among Jews.
Fried K
Isr J Med Sci; 1973; 9(9):1399. PubMed ID: 4775123
[No Abstract] [Full Text] [Related]
19. A large family with type IV radial polydactyly.
Seyhan A; Akarsu N; Keskin F
J Hand Surg Br; 1998 Aug; 23(4):530-3. PubMed ID: 9726561
[TBL] [Abstract][Full Text] [Related]
20. Holt-Oram syndrome with associated postaxial and central polydactyly. Further evidence for genetic heterogeneity in the Holt-Oram syndrome.
Fryns JP; Bonnet D; De Smet L
Genet Couns; 1996; 7(4):323-4. PubMed ID: 8985738
[No Abstract] [Full Text] [Related]
[Next] [New Search]
