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 *

85 related articles for article (PubMed ID: 7018242)

  • 21. 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]  

  • 22. Split--hand and split--foot deformity report of a family with 16 affected individuals in three generations.
    Sirinavin C; Kiratihatayakorn S; Nimmannit S; Issaragrisil S; Vidhayakom S
    J Med Assoc Thai; 1980 Mar; 63(3):121-9. PubMed ID: 7373184
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. Frameshift mutation in the cartilage-derived morphogenetic protein 1 (CDMP1) gene and severe acromesomelic chondrodysplasia resembling Grebe-type chondrodysplasia.
    Faiyaz-Ul-Haque M; Ahmad W; Wahab A; Haque S; Azim AC; Zaidi SH; Teebi AS; Ahmad M; Cohn DH; Siddique T; Tsui LC
    Am J Med Genet; 2002 Jul; 111(1):31-7. PubMed ID: 12124730
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Acheiropodia is caused by a genomic deletion in C7orf2, the human orthologue of the Lmbr1 gene.
    Ianakiev P; van Baren MJ ; Daly MJ; Toledo SP; Cavalcanti MG; Neto JC; Silveira EL; Freire-Maia A; Heutink P; Kilpatrick MW; Tsipouras P
    Am J Hum Genet; 2001 Jan; 68(1):38-45. PubMed ID: 11090342
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal father.
    De Smet L; Devriendt K; Fryns JP
    Genet Couns; 2001; 12(3):251-4. PubMed ID: 11693788
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder.
    Cantú JM; Rivera H; Nazará Z; Rojas Q; Hernández A; García-Cruz D
    Clin Genet; 1980 Sep; 18(3):153-9. PubMed ID: 7192193
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation.
    Dobbs MB; Gurnett CA; Robarge J; Gordon JE; Morcuende JA; Bowcock AM
    J Orthop Res; 2005 Nov; 23(6):1490-4. PubMed ID: 16005596
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Autosomal recessive type of whistling face syndrome in twins.
    Kousseff BG; McConnachie P; Hadro TA
    Pediatrics; 1982 Mar; 69(3):328-31. PubMed ID: 7199706
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Acheiropodia: new cases from Brazil.
    Silveira EL; Freire-Maia A
    Clin Genet; 1998 Sep; 54(3):256-7. PubMed ID: 9788736
    [No Abstract]   [Full Text] [Related]  

  • 32. Discrepancies in upper and lower limb patterning in split hand foot malformation.
    Elliott AM; Reed MH; Roscioli T; Evans JA
    Clin Genet; 2005 Nov; 68(5):408-23. PubMed ID: 16207208
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Costello syndrome and facio-cutaneous-skeletal syndrome.
    Philip N; Mancini J
    Am J Med Genet; 1993 Aug; 47(2):174-5. PubMed ID: 8213902
    [No Abstract]   [Full Text] [Related]  

  • 34. [Cryptorchidism with didymo-epididymal dissociation and Robinow's syndrome: 2 case reports].
    Fabbro MA; D'Agostino S; Costa L; Musi L; Cappellari F
    Pediatr Med Chir; 1997; 19(2):121-4. PubMed ID: 9312747
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Newly recognized autosomal recessive faciothoracoskeletal syndrome.
    Richieri-Costa A; Guion-Almeida ML; Lauris JR; Ferreira DM
    Am J Med Genet; 1994 Jan; 49(2):224-8. PubMed ID: 8116673
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness.
    Lezirovitz K; Pardono E; de Mello Auricchio MT; de Carvalho E Silva FL; Lopes JJ; Abreu-Silva RS; Romanos J; Batissoco AC; Mingroni-Netto RC
    Eur J Hum Genet; 2008 Jan; 16(1):89-96. PubMed ID: 17851452
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
    Teebi AS; Kaurah P
    Am J Med Genet; 1996 Dec; 66(3):257-60. PubMed ID: 8985482
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Urinary mucopolysaccharides in acheiropodia].
    Mourão PA; Toledo SP; Dietrich CP
    Rev Hosp Clin Fac Med Sao Paulo; 1977 Aug; 32(4):229-31. PubMed ID: 146906
    [No Abstract]   [Full Text] [Related]  

  • 40. Peters'-Plus syndrome with agenesis of the corpus callosum: report of a case and confirmation of autosomal recessive inheritance.
    Camera G; Centa A; Pozzolo S; Camera A
    Clin Dysmorphol; 1993 Oct; 2(4):317-21. PubMed ID: 8305962
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.