These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 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]
    of 7.