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 *

100 related articles for article (PubMed ID: 8723087)

  • 41. Bilateral asymmetry in cone epiphysis of the middle phalanx, fifth finger.
    Wetherington RK
    Am J Phys Anthropol; 1983 Mar; 60(3):319-21. PubMed ID: 6846506
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Osteopathia striata syndrome. Clinical, genetic and radiologic considerations.
    Bass HN; Weiner JR; Goldman A; Smith LE; Sparkes RS; Crandall BF
    Clin Pediatr (Phila); 1980 May; 19(5):369-73. PubMed ID: 6965904
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Spondylometaphyseal dysplasia-Sedaghatian type.
    Elçioglu N; Hall CM
    Am J Med Genet; 1998 Apr; 76(5):410-4. PubMed ID: 9556300
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Some roentgenological changes in the metaphyseal and epiphyseal zones during disturbances of general body growth in length].
    Tikhonov VA
    Vestn Rentgenol Radiol; 1967; 42(6):52-8. PubMed ID: 5616474
    [No Abstract]   [Full Text] [Related]  

  • 45. Michels syndrome in a Brazilian girl born to consanguineous parents.
    Guion-Almeida ML; Rodini ES
    Am J Med Genet; 1995 Jul; 57(3):377-9. PubMed ID: 7677137
    [TBL] [Abstract][Full Text] [Related]  

  • 46. An unclassifiable type of spondylo-peripheral epiphyseal dysplasia associated with 21 trisomy.
    Ioan DM; Popa M; Fryns JP
    Genet Couns; 1993; 4(1):59-62. PubMed ID: 8471223
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Syndrome of cleft palate, microcephaly, large ears, and short stature (Say syndrome).
    Abu-Libdeh B; Fujimoto A; Ehinger M
    Am J Med Genet; 1993 Feb; 45(3):358-60. PubMed ID: 8434624
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Spondylocarpotarsal synostosis with epiphyseal dysplasia.
    Honeywell C; Langer L; Allanson J
    Am J Med Genet; 2002 May; 109(4):318-22. PubMed ID: 11992487
    [TBL] [Abstract][Full Text] [Related]  

  • 49. New form of spondyloepimetaphyseal dysplasia (SEMD) in Jewish family of Iraqi origin.
    Shohat M; Lachman R; Carmi R; Bar Ziv J; Rimoin D
    Am J Med Genet; 1993 Jun; 46(4):358-62. PubMed ID: 8357004
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Compound heterozygosity for the Achondroplasia-hypochondroplasia FGFR3 mutations: prenatal diagnosis and postnatal outcome.
    Chitayat D; Fernandez B; Gardner A; Moore L; Glance P; Dunn M; Chun K; Sgro M; Ray P; Allingham-Hawkins D
    Am J Med Genet; 1999 Jun; 84(5):401-5. PubMed ID: 10360393
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Polymicrogyria, cerebellar vermis hypoplasia, severe facial dysmorphism and cleft palate: a new syndrome?
    Mosca AL; Laurent N; Guibaud L; Callier P; Thauvin-Robinet C; Mugneret F; Huet F; Grimaldi M; Gouyon JB; Sandre D; Faivre L
    Eur J Med Genet; 2007; 50(1):48-53. PubMed ID: 17067864
    [TBL] [Abstract][Full Text] [Related]  

  • 52. TAR syndrome with orofacial clefting.
    Midro A; Hubert E; Preferansow J; Iwaszkiewicz-Pawłowska A
    Genet Couns; 1993; 4(3):187-92. PubMed ID: 8267925
    [TBL] [Abstract][Full Text] [Related]  

  • 53. The Weissenbacher-Zweymuller syndrome of micrognathia and rhizomelic chondrodysplasia at birth with subsequent normal growth.
    Haller JO; Berdon WE; Robinow M; Slovis TL; Baker DH; Johnson GF
    Am J Roentgenol Radium Ther Nucl Med; 1975 Dec; 125(4):936-43. PubMed ID: 813535
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Generalized dysplasia of epiphyseal and metaphyseal exostoses in the Rubinstein-Taybi syndrome].
    Brandner M; Saur G
    Fortschr Geb Rontgenstr Nuklearmed; 1972 Sep; 117(3):317-23. PubMed ID: 4342581
    [No Abstract]   [Full Text] [Related]  

  • 55. Sedaghatian congenital lethal metaphyseal chondrodysplasia--observations in a second Iranian family and histopathological studies.
    Opitz JM; Spranger JW; Stöss HR; Pesch HJ; Azadeh B
    Am J Med Genet; 1987 Mar; 26(3):583-90. PubMed ID: 3565474
    [TBL] [Abstract][Full Text] [Related]  

  • 56. A new acro-cranio-facial dysostosis syndrome in sisters.
    Kaplan P; Plauchu H; Fitch N; Jéquier S
    Am J Med Genet; 1988 Jan; 29(1):95-106. PubMed ID: 3344780
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [The child with lip, maxillary, palatal cleft].
    Godbersen GS
    Laryngorhinootologie; 1997 Sep; 76(9):562-7. PubMed ID: 9417187
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Congenital bone diseases in newborn infants].
    Shimada N; Minowa H; Yanagida T
    Sanfujinka No Jissai; 1969 Jul; 18(7):641-50. PubMed ID: 5395331
    [No Abstract]   [Full Text] [Related]  

  • 59. Multiple epiphyseal dysplasia and Turner syndrome variant (45,XO/46,X ring) associated with advanced maternal age.
    Lowry RB; Wood BJ
    Birth Defects Orig Artic Ser; 1977; 13(3C):211-20. PubMed ID: 890113
    [No Abstract]   [Full Text] [Related]  

  • 60. Wolcott-Rallison syndrome.
    Juneja A; Sultan A; Bhatnagar S
    J Indian Soc Pedod Prev Dent; 2012; 30(3):250-3. PubMed ID: 23263430
    [TBL] [Abstract][Full Text] [Related]  

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