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 *

164 related articles for article (PubMed ID: 8415199)

  • 21. Femoral hypoplasia-unusual facies syndrome.
    Singh SK; Chandra D; Ravi RN; Kumari S
    Indian Pediatr; 1997 Aug; 34(8):747-8. PubMed ID: 9492409
    [No Abstract]   [Full Text] [Related]  

  • 22. [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]  

  • 23. A further case of a new syndrome including midface retraction, hypertrichosis, and skeletal anomalies.
    Donnai D; Harris R
    J Med Genet; 1979 Dec; 16(6):483-6. PubMed ID: 537022
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The Schinzel-Giedion syndrome. A case report and review of the literature.
    Pul M; Yilmaz N; Komsuoglu B
    Clin Pediatr (Phila); 1990 Apr; 29(4):235-9. PubMed ID: 2184969
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Acrofacial dysostoses.
    Le Merrer M; Cikuli M; Ribier J; Briard ML
    Am J Med Genet; 1989 Jul; 33(3):318-22. PubMed ID: 2801764
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome).
    Ruggieri M; Roggini M; Kennerknecht I; Polizzi A; Distefano A; Pavone V
    Acta Paediatr; 2011 Jan; 100(1):121-7. PubMed ID: 21143296
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Skeletal anomalies and ophthalmic findings in two siblings.
    Simonetos GA; Palimeris G
    Metab Pediatr Ophthalmol; 1981; 5(1):21-5. PubMed ID: 6973050
    [No Abstract]   [Full Text] [Related]  

  • 28. Picture of the month. Keutel syndrome.
    Tüysüz B; Ungür S; Akalin F; Cenani A; Tunnessen WW
    Arch Pediatr Adolesc Med; 1999 Jul; 153(7):765-6. PubMed ID: 10401814
    [No Abstract]   [Full Text] [Related]  

  • 29. Congenital glenoid dysplasia.
    Currarino G; Sheffield E; Twickler D
    Pediatr Radiol; 1998 Jan; 28(1):30-7. PubMed ID: 9426270
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Congenital malformations associated with maternal osteodysplasty. A new malformation complex.
    Theander G; Ekberg O
    Acta Radiol Diagn (Stockh); 1981; 22(3B):369-77. PubMed ID: 7304261
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cumming syndrome: report of two additional cases.
    Dibbern KM; Graham JM; Lachman RS; Wilcox WR
    Pediatr Radiol; 1998 Oct; 28(10):798-801. PubMed ID: 9799304
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Thin ribs, thin tubular bones, abnormal facies and intrauterine growth retardation: a lethal syndrome.
    Sharma BK; Kapoor R; Ramji S; Thirupuram S; Suri M
    Br J Radiol; 1990 Aug; 63(752):654-6. PubMed ID: 2400886
    [No Abstract]   [Full Text] [Related]  

  • 33. Skeletal anomalies in genetically determined congenital heart disease.
    Poznanski AK; Stern AM; Gall JC
    Radiol Clin North Am; 1971 Dec; 9(3):435-58. PubMed ID: 5145748
    [No Abstract]   [Full Text] [Related]  

  • 34. Acromesomelic dysplasia.
    Langer LO; Garrett RT
    Radiology; 1980 Nov; 137(2):349-55. PubMed ID: 7433666
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The Pointer syndrome: a new syndrome with skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficulties.
    Huq AH; Braverman RM; Greenberg F; Bacino CA; Rimoin DL; Lachman RS; Levin ML
    Am J Med Genet; 1997 Jan; 68(2):225-30. PubMed ID: 9028464
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Spondylo-epi-metaphyseal dysplasia with myotonia. A radiographic study. (Catel-Hempel syndrome, Schwarz-Jampel syndrome, Aberfeld syndrome, chondrodystrophic myotonia).
    Kozlowski K; Wise G
    Radiol Diagn (Berl); 1974; 15(6):817-24. PubMed ID: 4464536
    [No Abstract]   [Full Text] [Related]  

  • 37. [Radiological study of trisomy 8 mosaïcism (author's transl)].
    Grünebaum M; Tieder M
    Ann Radiol (Paris); 1976 Oct; 19(6):593-7. PubMed ID: 1015765
    [No Abstract]   [Full Text] [Related]  

  • 38. Asphyxiating thoracic dystrophy without respiratory disease.
    Karski T; Kozlowski K; Wrona J
    Radiol Med; 1993 Sep; 86(3):347-9. PubMed ID: 8210547
    [No Abstract]   [Full Text] [Related]  

  • 39. [Osteopathia striata: a characteristic roentgen finding in focal dermal hypoplasia (Goltz-Gorlin syndrome)].
    Barthels W; Boepple D; Petzel H
    Radiologe; 1982 Dec; 22(12):562-5. PubMed ID: 7156390
    [No Abstract]   [Full Text] [Related]  

  • 40. Syndrome of dental anomalies, curly hair and sclerotic bones.
    Lichtenstein JR; Warson RW
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):308-11. PubMed ID: 5173238
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.