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 *

139 related articles for article (PubMed ID: 7802046)

  • 1. Ectrodactyly and 7q22.1.
    Rivera H
    Am J Med Genet; 1994 Oct; 53(1):89-90. PubMed ID: 7802046
    [No Abstract]   [Full Text] [Related]  

  • 2. Inverted insertion of chromosome 7q and ectrodactyly.
    Naritomi K; Izumikawa Y; Tohma T; Hirayama K
    Am J Med Genet; 1993 Jun; 46(5):492-3. PubMed ID: 8322806
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ectrodactyly of hands and feet in a child with a complex translocation including 7q21.2.
    Sharland M; Patton MA; Hill L
    Am J Med Genet; 1991 Jun; 39(4):413-4. PubMed ID: 1877619
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Split hand/split foot anomaly in a family segregating a balanced translocation with breakpoint on 7q22.1.
    Genuardi M; Pomponi MG; Sammito V; Bellussi A; Zollino M; Neri G
    Am J Med Genet; 1993 Nov; 47(6):823-31. PubMed ID: 8279479
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ectrodactyly and proximal/intermediate interstitial deletion 7q.
    McElveen C; Carvajal MV; Moscatello D; Towner J; Lacassie Y
    Am J Med Genet; 1995 Mar; 56(1):1-5. PubMed ID: 7747769
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Triphalangeal thumb and split foot in the same family.
    Le Marec B; Odent S; Treguier C
    Genet Couns; 1990; 1(3-4):251-8. PubMed ID: 2098049
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Counseling dilemmas in EEC syndrome.
    Tekin M; Ohle C; Johnson DE; Christmas JT; Bodurtha J
    Genet Couns; 2000; 11(1):19-24. PubMed ID: 10756423
    [TBL] [Abstract][Full Text] [Related]  

  • 8. On the inheritance of the split hand/split foot malformation.
    Zlotogora J
    Am J Med Genet; 1994 Oct; 53(1):29-32. PubMed ID: 7802032
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Six generations of a family with multiple limb deficiencies.
    Helal A; Perry T; Ogden JA; Greene TL
    J Pediatr Orthop; 1993; 13(2):210-3. PubMed ID: 8459013
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ectrodactyly and absence (hypoplasia) of the tibia: are there dominant and recessive types?
    Majewski E; Goecke T; Meinecke P
    Am J Med Genet; 1996 May; 63(1):185-9. PubMed ID: 8723107
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Adermatoglyphia or "immigration delay disease": the role of mutations in the SMARCAD1 gene].
    Dereure O
    Ann Dermatol Venereol; 2012 Jan; 139(1):75-6. PubMed ID: 22225750
    [No Abstract]   [Full Text] [Related]  

  • 12. Monosomy 5p and trisomy 12p in a boy with familial balanced translocation.
    Vasudevan PC; Parker MJ
    Clin Dysmorphol; 2006 Apr; 15(2):85-7. PubMed ID: 16531734
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Heterogeneity of the autosomal dominant split hand/split foot malformation.
    Zlotogora J
    Am J Hum Genet; 1995 Jan; 56(1):341-3. PubMed ID: 7825599
    [No Abstract]   [Full Text] [Related]  

  • 14. Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3.
    Ignatius J; Knuutila S; Scherer SW; Trask B; Kere J
    J Med Genet; 1996 Jun; 33(6):507-10. PubMed ID: 8782053
    [TBL] [Abstract][Full Text] [Related]  

  • 15. p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly.
    Berdón-Zapata V; Granillo-Alvarez M; Valdés-Flores M; García-Ortiz JE; Kofman-Alfaro S; Zenteno JC
    J Orthop Res; 2004 Jan; 22(1):1-5. PubMed ID: 14656652
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exclusion of linkage between autosomal dominant split hand/split foot and markers from chromosome 7q: further evidence for genetic heterogeneity.
    Gurrieri F; Genuardi M; Chiurazzi P; Gillessen-Kaesbach G; Neri G
    Am J Hum Genet; 1994 Oct; 55(4):853-5. PubMed ID: 7942863
    [No Abstract]   [Full Text] [Related]  

  • 17. Ectrodactyly in trisomy 13 syndrome.
    Urioste M; Martínez-Frías ML; Aparicio P
    Am J Med Genet; 1994 Dec; 53(4):390-2. PubMed ID: 7864055
    [No Abstract]   [Full Text] [Related]  

  • 18. Autosomal dominant ectrodactyly with sensorineural deafness.
    Mishra P; Muranjan M; Bharucha BA
    Clin Dysmorphol; 2000 Apr; 9(2):119-21. PubMed ID: 10826624
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genes for split hand/split foot and laterality defects on 7q22.1 and Xq24-q27.1.
    Genuardi M; Gurrieri F; Neri G
    Am J Med Genet; 1994 Mar; 50(1):101. PubMed ID: 8160746
    [No Abstract]   [Full Text] [Related]  

  • 20. A split hand-split foot (SHFM3) gene is located at 10q24-->25.
    Gurrieri F; Prinos P; Tackels D; Kilpatrick MW; Allanson J; Genuardi M; Vuckov A; Nanni L; Sangiorgi E; Garofalo G; Nunes ME; Neri G; Schwartz C; Tsipouras P
    Am J Med Genet; 1996 Apr; 62(4):427-36. PubMed ID: 8723077
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.