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 *

213 related articles for article (PubMed ID: 1416547)

  • 21. Desbuquois dysplasia, a reevaluation with abnormal and "normal" hands: radiographic manifestations.
    Faivre L; Cormier-Daire V; Eliott AM; Field F; Munnich A; Maroteaux P; Le Merrer M; Lachman R
    Am J Med Genet A; 2004 Jan; 124A(1):48-53. PubMed ID: 14679586
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Extra pelvic ossification centers in thanatophoric dysplasia and platyspondylic lethal skeletal dysplasia-San Diego type.
    Kitoh H; Lachman RS; Brodie SG; Mekikian PB; Rimoin DL; Wilcox WR
    Pediatr Radiol; 1998 Oct; 28(10):759-63. PubMed ID: 9799297
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Spondylo-metaphyseal dysplasia Algerian type: confirmation of a new syndrome.
    Rybak M; Foley TP; Kozlowski K
    Am J Med Genet; 1991 Sep; 40(3):304-6. PubMed ID: 1951433
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Jarcho-Levin syndrome: report of three cases. Associated extra-skeletal malformations].
    Cañabate Reche F; González-Ripoll Garzón M; Martín González M; López Muñoz J
    An Esp Pediatr; 1993 Jan; 38(1):54-6. PubMed ID: 8439081
    [No Abstract]   [Full Text] [Related]  

  • 25. Morphologic observations in a case of lethal variant (type I) metatropic dysplasia with atypical features: morphology of lethal metatropic dysplasia.
    O'Sullivan MJ; McAllister WH; Ball RH; Teitelbaum SL; Swanson PE; Dehner LP
    Pediatr Dev Pathol; 1998; 1(5):405-12. PubMed ID: 10507892
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Fibrochondrogenesis: radiologic and histologic studies.
    Eteson DJ; Adomian GE; Ornoy A; Koide T; Sugiura Y; Calabro A; Lungarotti S; Mastroiacovo P; Lachman RS; Rimoin DL
    Am J Med Genet; 1984 Oct; 19(2):277-90. PubMed ID: 6507479
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2.
    Cormier-Daire V; Superti-Furga A; Munnich A; Lyonnet S; Rustin P; Delezoide AL; De Lonlay P; Giedion A; Maroteaux P; Le Merrer M
    Am J Med Genet; 1998 Jun; 78(2):146-9. PubMed ID: 9674905
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [A case of type II achondrogenesis].
    Micheli E; Perrone C; Quarta Colosso L; Vetrugno M; Zecca G; Indirli GC; Greco F; Elia G; Ciancio S
    Pediatr Med Chir; 1996; 18(1):105-7. PubMed ID: 8685014
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Patterson-Lowry rhizomelic dysplasia: a potentially lethal bone dysplasia?
    Kamoda T; Nakajima R; Matsui A; Nishimura G
    Pediatr Radiol; 2001 Feb; 31(2):81-3. PubMed ID: 11214690
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A case of acampomelic campomelic dysplasia.
    Ozkilic A; Seven M; Yuksel A
    Genet Couns; 2002; 13(1):23-8. PubMed ID: 12017234
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Atelosteogenesis.
    Maroteaux P; Spranger J; Stanescu V; Le Marec B; Pfeiffer RA; Beighton P; Mattei JF
    Am J Med Genet; 1982 Sep; 13(1):15-25. PubMed ID: 7137218
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital neuroblastoma in a neonate with hypoparathyroidism-retardation-dysmorphism syndrome.
    Golan-Tripto I; Ling E; Hershkovitz E; Fruchtman Y; Hazan G
    Clin Dysmorphol; 2020 Jan; 29(1):46-48. PubMed ID: 31205051
    [No Abstract]   [Full Text] [Related]  

  • 33. Leg duplication and kidney agenesis: case report and pathogenic considerations.
    Van Groesen PJ; Beemer FA; Van de Kamp JH
    Genet Couns; 1990; 1(3-4):265-72. PubMed ID: 2098051
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Differentiating campomelic dysplasia from Cumming syndrome.
    Watiker V; Lachman RS; Wilcox WR; Barroso I; Schafer AJ; Scherer G
    Am J Med Genet A; 2005 May; 135(1):110-2. PubMed ID: 15754354
    [No Abstract]   [Full Text] [Related]  

  • 35. Osteochondrodysplasia in Fryns syndrome.
    Kershisnik MM; Craven CM; Jung AL; Carey JC; Knisely AS
    Am J Dis Child; 1991 Jun; 145(6):656-60. PubMed ID: 1903587
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prevalence of lethal osteochondrodysplasias in Denmark.
    Andersen PE
    Am J Med Genet; 1989 Apr; 32(4):484-9. PubMed ID: 2789000
    [TBL] [Abstract][Full Text] [Related]  

  • 37. New form of platyspondylic lethal chondrodysplasia.
    Akaba K; Nishimura G; Hashimoto M; Wakabayashi T; Kanasugi H; Hayasaka K
    Am J Med Genet; 1996 Dec; 66(4):464-7. PubMed ID: 8989469
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Surviving campomelic dysplasia has the radiological features of the previously reported ischio-pubic-patella syndrome.
    Offiah AC; Mansour S; McDowall S; Tolmie J; Sim P; Hall CM
    J Med Genet; 2002 Sep; 39(9):e50. PubMed ID: 12205120
    [No Abstract]   [Full Text] [Related]  

  • 39. Acampomelic campomelic dysplasia with de novo 5q;17q reciprocal translocation and severe phenotype.
    Savarirayan R; Bankier A
    J Med Genet; 1998 Jul; 35(7):597-9. PubMed ID: 9678706
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Metacarpophalangeal pattern profile analysis in diastrophic dysplasia.
    Butler MG; Gale DD; Meaney FJ
    Am J Med Genet; 1987 Nov; 28(3):685-9. PubMed ID: 3425635
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.