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 *

113 related articles for article (PubMed ID: 11045581)

  • 1. A syndrome with midface asymmetry, defective modelling of the skeleton, catch-up growth and truncal obesity.
    Kajantie E; Pirinen S; Tommiska V; Kaitila I
    Clin Dysmorphol; 2000 Oct; 9(4):259-64. PubMed ID: 11045581
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation: a new syndrome?
    Zerres K; Rietschel M; Rietschel E; Majewski F; Meinecke P
    J Med Genet; 1992 Apr; 29(4):269-71. PubMed ID: 1316441
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Patellar dislocation in Kabuki syndrome.
    Kurosawa K; Kawame H; Ochiai Y; Nakashima M; Tohma T; Ohashi H
    Am J Med Genet; 2002 Mar; 108(2):160-3. PubMed ID: 11857567
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Midface hypoplasia, obesity, developmental delay and neonatal hypotonia in two brothers.
    Rozendaal L; Del Canho H; Waterham HR; Hennekam RC
    Clin Dysmorphol; 2003 Jan; 12(1):9-13. PubMed ID: 12514359
    [TBL] [Abstract][Full Text] [Related]  

  • 5. KBG syndrome.
    Brancati F; Sarkozy A; Dallapiccola B
    Orphanet J Rare Dis; 2006 Dec; 1():50. PubMed ID: 17163996
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unusual type of brachydactyly associated with short stature and facial anomalies. A new syndrome?
    Richieri-Costa A; Colletto GM; Otto PA
    Am J Med Genet; 1985 Aug; 21(4):637-42. PubMed ID: 4025394
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Schinzel-Giedion-like syndrome--a milder version or a separate condition?
    Joss S; Dean JC
    Clin Dysmorphol; 2002 Oct; 11(4):271-5. PubMed ID: 12401993
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Kivlin syndrome and Peters'-Plus syndrome: are they the same disorder?
    Thompson EM; Winter RM; Baraitser M
    Clin Dysmorphol; 1993 Oct; 2(4):301-16. PubMed ID: 7508317
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypertrichosis, coarse face, brachydactyly, obesity and mental retardation.
    Pavone L; Rizzo R; Ruggieri M; Sorge G
    Clin Dysmorphol; 1996 Jul; 5(3):223-9. PubMed ID: 8818451
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Short stature, moderate mental retardation, hyperactivity, facial dysmorphism, skeletal abnormalities, and exaggerated ketosis: a new syndrome.
    Boneh A; Glick B; Gutman A; Mogle P
    Clin Genet; 1996 Nov; 50(5):403-6. PubMed ID: 9007332
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A syndrome of severe midface retraction, multiple skull anomalies, clubfeet, and cardiac and renal malformations in sibs.
    Schinzel A; Giedion A
    Am J Med Genet; 1978; 1(4):361-75. PubMed ID: 665725
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An unknown autoinflammatory syndrome associated with short stature and dysmorphic features in a young boy.
    Mégarbané A; Sanders A; Chouery E; Delague V; Medlej-Hashim M; Torbey PH
    J Rheumatol; 2002 May; 29(5):1084-7. PubMed ID: 12022327
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype.
    Tekin M; Kavaz A; Berberoğlu M; Fitoz S; Ekim M; Ocal G; Akar N
    Am J Med Genet A; 2004 Oct; 130A(3):284-7. PubMed ID: 15378538
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Greig's syndrome. Neonatal radiologic manifestations].
    Merlob P; Grunebaum M; Mimouni F; Reisner SH
    J Radiol; 1984 Mar; 65(3):187-9. PubMed ID: 6325685
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Schinzel-Giedion syndrome: autopsy report and additional clinical manifestations.
    Rodríguez JI; Jiménez-Heffernan JA; Leal J
    Am J Med Genet; 1994 Dec; 53(4):374-7. PubMed ID: 7864048
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Thirty-two year follow-up of the first patient reported with the Floating-Harbor syndrome.
    Feingold M
    Am J Med Genet A; 2006 Apr; 140(7):782-4. PubMed ID: 16523514
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay.
    Feingold M; Hall BD; Lacassie Y; Martínez-Frías ML
    Am J Med Genet; 1997 Mar; 69(3):245-9. PubMed ID: 9096752
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Natural history and postmortem anatomy of a patient with tetra-amelia, ectodermal dysplasia, peculiar face, and developmental retardation (MIM 273390).
    Ohdo S; Sonoda T; Ohba K
    J Med Genet; 1994 Dec; 31(12):980-1. PubMed ID: 7534355
    [No Abstract]   [Full Text] [Related]  

  • 19. Unknown syndrome: nasal hypoplasia, sparse hair, truncal obesity, genital hypoplasia, and severe mental retardation.
    Fryns JP; Delooz J; Van Den Berghe H
    J Med Genet; 1992 Sep; 29(9):676-7. PubMed ID: 1404303
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A patient with Schinzel-Giedion syndrome and a review of 20 patients.
    Okamoto N; Takeuchi M; Kitajima H; Hosokawa S
    Jpn J Hum Genet; 1995 Jun; 40(2):189-93. PubMed ID: 7662999
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.