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: 7700715)

  • 21. Mendel might get dizzy.
    Hall JG
    CMAJ; 1997 Dec; 157(12):1669-70. PubMed ID: 9418653
    [No Abstract]   [Full Text] [Related]  

  • 22. Auxological and anthropometric evaluation in skeletal dysplasias.
    Mazzanti L; Matteucci C; Scarano E; Tamburrino F; Ragni MC; Cicognani A
    J Endocrinol Invest; 2010 Jun; 33(6 Suppl):19-25. PubMed ID: 21057181
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Skeletal dysplasias detectable by DNA analysis.
    Reardon W
    Prenat Diagn; 1996 Dec; 16(13):1221-36. PubMed ID: 9061753
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Phenotypic differences in Angelman syndrome patients: imprinting mutations show less frequently microcephaly and hypopigmentation than deletions.
    Bürger J; Kunze J; Sperling K; Reis A
    Am J Med Genet; 1996 Dec; 66(2):221-6. PubMed ID: 8958335
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetics beyond Mendel. Understanding nontraditional inheritance patterns.
    Wagstaff J
    Postgrad Med; 2000 Sep; 108(3):131-3, 137-8. PubMed ID: 11004940
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Skeletal dysplasias and the growth plate.
    Alman BA
    Clin Genet; 2008 Jan; 73(1):24-30. PubMed ID: 18070126
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Bone dysplasias: the A, B, C of radiographic interpretation.
    Castriota-Scanderbeg A
    J Endocrinol Invest; 2010 Jun; 33(6 Suppl):26-9. PubMed ID: 21057182
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Grandpaternal mosaicism in a family with isolated haemophilia A.
    Casey GJ; Rodgers SE; Hall JR; Rudzki Z; Lloyd JV
    Br J Haematol; 1999 Dec; 107(3):560-2. PubMed ID: 10583258
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A family with whistling-face-syndrome.
    Wettstein A; Buchinger G; Braun A; von Bazan UB
    Hum Genet; 1980; 55(2):177-89. PubMed ID: 7450762
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A pair of siblings with diastrophic dysplasia and E trisomy mosaicism.
    Holmgren G; Jagell S; Lagerkvist B; Nordenson I
    Hum Hered; 1984; 34(4):266-8. PubMed ID: 6479995
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes.
    Duchatelet S; Ostergaard E; Cortes D; Lemainque A; Julier C
    Hum Mol Genet; 2005 Jan; 14(1):1-5. PubMed ID: 15525660
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Craniosynostosis and skeletal dysplasias: fibroblast growth factor receptor defects.
    Lewanda AF; Meyers GA; Jabs EW
    Proc Assoc Am Physicians; 1996 Jan; 108(1):19-24. PubMed ID: 8834060
    [No Abstract]   [Full Text] [Related]  

  • 33. The Dyggve-Melchior-Clausen syndrome in Indian siblings.
    Winship WS; Rubin DL
    Clin Genet; 1992 Nov; 42(5):240-5. PubMed ID: 1486701
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical use of "somatometric profiles" and the effect of polygenic inheritance for stature in patients with bone dysplasias.
    Guízar-Vázquez J; Ramírez-Gutiérrez V; Zavala C; Salamanca F
    Rev Invest Clin; 1983; 35(3):231-5. PubMed ID: 6635384
    [No Abstract]   [Full Text] [Related]  

  • 35. [Current interpretation of mosaicism].
    Méhes K; Kosztolányi G
    Orv Hetil; 1990 Aug; 131(33):1815-9. PubMed ID: 2204862
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel MSP/DHPLC method for the investigation of the methylation status of imprinted genes enables the molecular detection of low cell mosaicisms.
    Baumer A; Wiedemann U; Hergersberg M; Schinzel A
    Hum Mutat; 2001 May; 17(5):423-30. PubMed ID: 11317358
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Skeletal dysplasias: New medical treatments].
    Argente J; Martos Moreno GÁ
    An Pediatr (Barc); 2016 Jul; 85(1):1-3. PubMed ID: 27117538
    [No Abstract]   [Full Text] [Related]  

  • 38. Maternally inherited duplication of the possible imprinted 14q31 region.
    Mignon-Ravix C; Mugneret F; Stavropoulou C; Depetris D; Khau Van Kien P; Mattei MG
    J Med Genet; 2001 May; 38(5):343-7. PubMed ID: 11403046
    [No Abstract]   [Full Text] [Related]  

  • 39. Thoughts on some new and old bone dysplasias.
    Gorlin RJ
    Prog Clin Biol Res; 1982; 104():47-52. PubMed ID: 7163286
    [No Abstract]   [Full Text] [Related]  

  • 40. Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting.
    Kotzot D
    Ann Genet; 2004; 47(3):251-60. PubMed ID: 15337470
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.