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 *

156 related articles for article (PubMed ID: 7447519)

  • 21. The Perlman syndrome: clinical and biological aspects.
    Neri G; Martini-Neri ME; Opitz JM; Freed JJ
    Prog Clin Biol Res; 1985; 200():269-76. PubMed ID: 3001776
    [No Abstract]   [Full Text] [Related]  

  • 22. Short stature, abnormal face, joint laxity, dislocation, hernias, delayed bone age, and severe psychomotor retardation in two brothers: previously undescribed MCA/MR syndrome.
    Mégarbané A; Ruchoux MM; Loeys B; Ayoub N; Nuytinck L
    Am J Med Genet; 2001 Dec; 104(3):221-4. PubMed ID: 11754048
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Simpson-Golabi-Behmel syndrome. A new overgrowth syndrome with increased risk of tumor development].
    Weidle B; Orstavik KH
    Tidsskr Nor Laegeforen; 1998 Apr; 118(10):1556-8. PubMed ID: 9615582
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Aarskog syndrome (author's transl)].
    Kunze J; Spranger J
    Klin Padiatr; 1973 Nov; 185(6):490-4. PubMed ID: 4798676
    [No Abstract]   [Full Text] [Related]  

  • 25. Autosomal dominant Russell-Silver syndrome.
    Al-Fifi S; Teebi AS; Shevell M
    Am J Med Genet; 1996 Jan; 61(1):96-7. PubMed ID: 8741931
    [No Abstract]   [Full Text] [Related]  

  • 26. Further delineation of the Simpson-Golabi-Behmel (SGB) syndrome.
    Lin AE
    Am J Med Genet; 1993 Jun; 46(5):606-7. PubMed ID: 8322829
    [No Abstract]   [Full Text] [Related]  

  • 27. [A case of leprechaunism with cryptorchidism].
    Yamaguchi T; Osada Y
    Hinyokika Kiyo; 1987 Nov; 33(11):1913-6. PubMed ID: 2895574
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Noonan's syndrome].
    Liashukh PI
    Vrach Delo; 1987 Jul; (7):52-3. PubMed ID: 3630122
    [No Abstract]   [Full Text] [Related]  

  • 29. Hypertrichosis, pigmentary retinopathy, and facial anomalies: a new syndrome?
    Pivnick EK; Wilroy RS; Martens PR; Teather TC; Hashimoto K
    Am J Med Genet; 1996 Apr; 62(4):386-90. PubMed ID: 8723069
    [TBL] [Abstract][Full Text] [Related]  

  • 30. CHARGE association.
    Toriello HV
    Ear Nose Throat J; 1999 Jun; 78(6):413. PubMed ID: 10388189
    [No Abstract]   [Full Text] [Related]  

  • 31. Studies on the pathogenesis of Costello syndrome.
    Mancini GM; van Diggelen OP; Kleijer WJ; Di Rocco M; Farina V; Yuksel-Apak M; Kayserili H; Halley DJ
    J Med Genet; 2003 Apr; 40(4):e37. PubMed ID: 12676910
    [No Abstract]   [Full Text] [Related]  

  • 32. [Potter-syndrome and sirenomelia (author's transl)].
    Gärtner H; Rosanelli K; Becker H
    Padiatr Padol; 1974; 9(3):209-16. PubMed ID: 4410459
    [No Abstract]   [Full Text] [Related]  

  • 33. Prenatal analysis of the insulin receptor gene in a family with leprechaunism.
    Longo N; Langley SD; Still MJ; Elsas LJ
    Prenat Diagn; 1995 Nov; 15(11):1070-4. PubMed ID: 8606887
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Another case of the autosomal recessive Weaver-like syndrome.
    Slaney SF; Winter RM
    Am J Med Genet; 1997 Oct; 72(3):369-70. PubMed ID: 9332672
    [No Abstract]   [Full Text] [Related]  

  • 35. Floating-Harbor syndrome in a Kuwaiti patient: a case report and literature review.
    Bastaki L; El-Nabi MM; Azab AS; Gouda SA; Al-Wadaani AM; Naguib KK
    East Mediterr Health J; 2007; 13(4):975-9. PubMed ID: 17955782
    [No Abstract]   [Full Text] [Related]  

  • 36. Reply to "lymphoproliferative disorders in Sotos syndrome: observation in two cases".
    Cole T; Allanson J
    Am J Med Genet; 1998 Jan; 75(2):226-7. PubMed ID: 9450893
    [No Abstract]   [Full Text] [Related]  

  • 37. Tricho-rhino-phalangeal syndrome type II: Langer-Giedion syndrome in a 2.5 years-old boy.
    Fryns JP; Emmery L; Timmermans J; Pedersen JC; van den Berghe H
    J Genet Hum; 1980 Mar; 28(1):53-6. PubMed ID: 7400785
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [A casuistic contribution to potter syndrome of dysplasia renofacialis with and without sirenomelia (author's transl)].
    Kühner U; Buchinger G; Fricke G; Romen H
    Klin Padiatr; 1976 May; 188(3):289-94. PubMed ID: 945426
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Roberts syndrome: study of 4 new Rgyptian cases with comparison of clinical and cytogenetic findings.
    Temtamy SA; Ismail S; Helmy NA
    Genet Couns; 2006; 17(1):1-13. PubMed ID: 16719272
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B; Ulmer H; Müller U
    Am J Med Genet; 1994 Apr; 50(2):173-6. PubMed ID: 8010348
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.