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 *

215 related articles for article (PubMed ID: 1897566)

  • 1. Osteodysplastic variant of primordial dwarfism.
    Shebib S; Hugosson C; Sakati N; Nyhan WL
    Am J Med Genet; 1991 Aug; 40(2):146-50. PubMed ID: 1897566
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Differential diagnostic considerations in microcephalic dwarfism].
    Kraft CN; Diedrich O; Wagner U; Schmitt O
    Z Orthop Ihre Grenzgeb; 2000; 138(2):126-30. PubMed ID: 10820877
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Studies of microcephalic primordial dwarfism II: the osteodysplastic type II of primordial dwarfism.
    Majewski F; Ranke M; Schinzel A
    Am J Med Genet; 1982 May; 12(1):23-35. PubMed ID: 7201238
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Microlissencephaly in microcephalic osteodysplastic primordial dwarfism: a case report and review of the literature.
    Klinge L; Schaper J; Wieczorek D; Voit T
    Neuropediatrics; 2002 Dec; 33(6):309-13. PubMed ID: 12571786
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Primordial osteodysplastic dwarfism type I in association with corneal clouding: evidence for autosomal recessive inheritance.
    Van Maldergem L; Gillerot Y; Godhaird M; Nemec E; Koulischer L
    Clin Genet; 1990 Nov; 38(5):359-61. PubMed ID: 2282715
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and genetic heterogeneity of Seckel syndrome.
    Faivre L; Le Merrer M; Lyonnet S; Plauchu H; Dagoneau N; Campos-Xavier AB; Attia-Sobol J; Verloes A; Munnich A; Cormier-Daire V
    Am J Med Genet; 2002 Nov; 112(4):379-83. PubMed ID: 12376940
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.
    Franceschini P; Testa A; Bogetti G; Girardo E; Guala A; Lopez-Bell G; Buzio G; Ferrario E; Piccato E
    Am J Med Genet; 1992 Jan; 42(1):112-6. PubMed ID: 1308349
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Caroline Crachami and the delineation of osteodysplastic primordial dwarfism type III, and autosomal recessive syndrome.
    Majewski F
    Am J Med Genet; 1992 Sep; 44(2):203-9. PubMed ID: 1456293
    [No Abstract]   [Full Text] [Related]  

  • 9. Pachygyria in a girl with microcephalic osteodysplastic primordial short stature type II.
    Ozawa H; Takayama C; Nishida A; Nagai T; Nishimura G; Higurashi M
    Brain Dev; 2005 Apr; 27(3):237-40. PubMed ID: 15737708
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Apparently new osteodysplastic and primordial short stature with severe microdontia, opalescent teeth, and rootless molars in two siblings.
    Kantaputra PN
    Am J Med Genet; 2002 Sep; 111(4):420-8. PubMed ID: 12210304
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Microcephalic osteodysplastic dwarfism (type II-like) in siblings.
    Verloes A; Lambrechts L; Senterre J; Lambotte C
    Clin Genet; 1987 Aug; 32(2):88-94. PubMed ID: 3652495
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome?
    Belengeanu V; Rozsnyai K; Farcaş S; Velea I; Fryns JP
    Genet Couns; 2005; 16(2):167-71. PubMed ID: 16080297
    [TBL] [Abstract][Full Text] [Related]  

  • 13. New syndromes of mental retardation.
    Thurmon TF; Santos CL
    Birth Defects Orig Artic Ser; 1975; 11(2):264-8. PubMed ID: 1227531
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Two Japanese cases with microcephalic primordial dwarfism: classical Seckel syndrome and osteodysplastic primordial dwarfism type II.
    Sugio Y; Tsukahara M; Kajii T
    Jpn J Hum Genet; 1993 Jun; 38(2):209-17. PubMed ID: 8358044
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal recessive severe dwarfism in a Sicilian girl: a new form of osteodysplastic primordial dwarfism?
    Corsello G; Albanese A; Piccione M; Giuffrè M; Opitz JM
    Am J Med Genet; 1996 Dec; 66(3):265-8. PubMed ID: 8985484
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cleft palate-lateral synechiae syndrome: report on three new patients with additional findings and evidence for variability and heterogeneity.
    Nakata NM; Guion-Almeida ML; Richieri-Costa A
    Am J Med Genet; 1993 Sep; 47(3):330-2. PubMed ID: 8135276
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cutaneous features associated with microcephalic osteodysplastic primordial dwarfism type II.
    Webber N; O'Toole EA; Paige DG; Rosser E
    Pediatr Dermatol; 2008; 25(3):401-2. PubMed ID: 18577061
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A new (brachymelic) type of primordial dwarfism (author's transl)].
    Majewski F; Spranger J
    Monatsschr Kinderheilkd (1902); 1976 Jun; 124(6):499-503. PubMed ID: 934161
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Microcephaly, micrognathia, and bird-headed dwarfism: prenatal diagnosis of a Seckel-like syndrome.
    Majoor-Krakauer DF; Wladimiroff JW; Stewart PA; van de Harten JJ; Niermeijer MF
    Am J Med Genet; 1987 May; 27(1):183-8. PubMed ID: 3300331
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Osteodysplastic primordial dwarfism: report of a further patient with manifestations similar to those seen in patients with types I and III.
    Winter RM; Wigglesworth J; Harding BN
    Am J Med Genet; 1985 Jul; 21(3):569-74. PubMed ID: 4025388
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.