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 *

118 related articles for article (PubMed ID: 8152878)

  • 41. Mental retardation and osteosclerosis.
    Hunter AG; Macpherson RI
    Am J Med Genet; 1978; 2(3):267-73. PubMed ID: 263443
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Craniovertebral junction stenosis in Lenz-Majewski syndrome.
    Mizuguchi K; Miyazaki O; Nishimura G; Ishigro A
    Pediatr Radiol; 2015 Sep; 45(10):1567-70. PubMed ID: 25779830
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Progressive facial disfigurement and deafness in craniometaphyseal dysplasia.
    Vasu CK; Rajendran VR; Regi George AN; Anoop P; Anjay MA
    Indian J Pediatr; 2006 Dec; 73(12):1105. PubMed ID: 17202639
    [No Abstract]   [Full Text] [Related]  

  • 44. [Spondylometaphyseal dysplasia type Kozlowski detected in family low body height].
    López ID; Estévez AR; Gonzalo AM; Jiménez JM
    Radiologia; 2008; 50(2):174. PubMed ID: 18367076
    [No Abstract]   [Full Text] [Related]  

  • 45. Acrodysostosis. A case of peripheral dysostosis, nasal hypoplasia, mental retardation and impaired hearing.
    Reiter S
    Pediatr Radiol; 1978 Apr; 7(1):53-5. PubMed ID: 643365
    [TBL] [Abstract][Full Text] [Related]  

  • 46. "Duplicate calcaneus": a rare developmental defect observed in several skeletal dysplasias.
    Cormier-Daire V; Savarirayan R; Unger S; Rimoin DL; Lachman RS
    Pediatr Radiol; 2001 Jan; 31(1):38-42. PubMed ID: 11200997
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Mental retardation, epilepsy, short stature, and skeletal dysplasia: confirmation of the Gurrieri syndrome.
    Battaglia A; Orsitto E; Gibilisco G
    Am J Med Genet; 1996 Mar; 62(3):230-2. PubMed ID: 8882779
    [TBL] [Abstract][Full Text] [Related]  

  • 48. [Importance of hand films in skeletal dysplasia (author's transl)].
    Fendel H
    Radiologe; 1976 Jul; 16(7):273-7. PubMed ID: 959512
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Cardiac involvement in geleophysic dysplasia in three siblings of a Saudi family.
    Elhoury ME; Faqeih E; Almoukirish AS; Galal MO
    Cardiol Young; 2015 Jan; 25(1):81-6. PubMed ID: 24192049
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Spondyloepiphyseal dysplasia tarda: a new autosomal recessive variant with mental retardation.
    Kohn G; Elrayyes ER; Makadmah I; Rösler A; Grünebaum M
    J Med Genet; 1987 Jun; 24(6):366-9. PubMed ID: 3612708
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Skeletal dysplasia and osseous maturation in hypothyroidism of childhood].
    Rybak M
    Ann Radiol (Paris); 1970; 13(3):243-9. PubMed ID: 5421908
    [No Abstract]   [Full Text] [Related]  

  • 52. Type A1 brachydactyly, dwarfism, ptosis, mixed partial hearing loss, microcephaly, and mental retardation.
    Tsukahara M; Azuno Y; Kajii T
    Am J Med Genet; 1989 May; 33(1):7-9. PubMed ID: 2750787
    [No Abstract]   [Full Text] [Related]  

  • 53. Dyggve-Melchiore-Clausen dysplasia (DMC): syndrome associated with a micropenis.
    Latrech H; Skiker I; Bentata Y; Alami Z; Mouhib Lav O; Oulali N; Benajiba N; Benmassoud S; El Jabri M; Gaouzi A; Gharbi MH; Chradibi A
    Pediatr Endocrinol Rev; 2013 Dec; 11(2):181-5. PubMed ID: 24575553
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Hajdu-Cheney syndrome: an unusual cause of acro-osteolysis].
    Bonneville F; Jomaah N; Le Hir P; Zeitoun F; Hamzé B; Arrivé L; Tubiana J
    J Radiol; 2000 Jul; 81(7):815-6. PubMed ID: 10915997
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Hirsutism-skeletal dysplasia-mental retardation syndrome with abnormal face and a uric acid metabolism disorder.
    Wiedemann HR; Oldigs HD; Oppermann HC; Oster O
    Am J Med Genet; 1993 Jun; 46(4):403-9. PubMed ID: 8357012
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Parental consanguinity in two sibs with omodysplasia.
    Baxová A; Maroteaux P; Barosová J; Netriová I
    Am J Med Genet; 1994 Feb; 49(3):263-5. PubMed ID: 8209882
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Spondylocostal dysostosis in South African sisters.
    Beighton P; Horan FT
    Clin Genet; 1981 Jan; 19(1):23-5. PubMed ID: 7460377
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Radiological and orthopedic abnormalities in Satoyoshi syndrome.
    Haymon M; Willis RB; Ehlayel MS; Lacassie Y
    Pediatr Radiol; 1997 May; 27(5):415-8. PubMed ID: 9133353
    [TBL] [Abstract][Full Text] [Related]  

  • 59. The wide spectrum of the asphyxiating thoracic dysplasia.
    Cortina H; Beltran J; Olague R; Ceres L; Alonso A; Lanuza A
    Pediatr Radiol; 1979 Apr; 8(2):93-9. PubMed ID: 450492
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Severe mental retardation, epilepsy, anal anomalies, and distal phalangeal hypoplasia in siblings.
    Marcelis CL; Rieu P; Beemer F; Brunner HG
    Clin Dysmorphol; 2007 Apr; 16(2):73-76. PubMed ID: 17351347
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.