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 *

136 related articles for article (PubMed ID: 6584558)

  • 21. Zimmermann-Laband syndrome in a patient with severe mental retardation.
    Van Buggenhout GJ; Brunner HG; Trommelen JC; Hamel BC
    Genet Couns; 1995; 6(4):321-7. PubMed ID: 8775419
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The genetics of human hair growth.
    Porter PS
    Birth Defects Orig Artic Ser; 1971 Jun; 7(8):69-85. PubMed ID: 5173315
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Pallister-Killian syndrome: a mild case diagnosed by fluorescence in situ hybridization. Review of the literature and expansion of the phenotype.
    Bielanska MM; Khalifa MM; Duncan AM
    Am J Med Genet; 1996 Oct; 65(2):104-8. PubMed ID: 8911599
    [TBL] [Abstract][Full Text] [Related]  

  • 24. FG syndrome: the trias mental retardation, hypotonia and constipation reviewed.
    Zwamborn-Hanssen AM; Schrander-Stumpel CT; Smeets E; Decock P; Fryns JP
    Genet Couns; 1995; 6(4):313-9. PubMed ID: 8775418
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Clinical considerations on a probable new case of the Coffin-Siris syndrome].
    D'Elia R; Cassone L; Senatore A; Scianaro L; Loiodice G
    Minerva Pediatr; 1981 Oct; 33(20):1021-4. PubMed ID: 7311957
    [No Abstract]   [Full Text] [Related]  

  • 26. Supernumerary chromosome der(22)t(11;22): Emanuel syndrome associates with novel features.
    Yosunkaya Fenerci E; Guven GS; Kuru D; Yilmaz S; Tarkan-Argüden Y; Cirakoglu A; Deviren A; Yüksel A; Hacihanefioğlu S
    Genet Couns; 2007; 18(4):401-8. PubMed ID: 18286821
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Gillespie syndrome: a report of two further cases.
    Nelson J; Flaherty M; Grattan-Smith P
    Am J Med Genet; 1997 Aug; 71(2):134-8. PubMed ID: 9217210
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cardio-facio-cutaneous (CFC) syndrome in a child carrying an inherited inversion of chromosome 7.
    Lopez-Rangel E; Hrynchak M; Friedman JM
    Am J Med Genet; 1993 Sep; 47(3):326-9. PubMed ID: 8135275
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Kinky hair disease--a new syndrome with cerebral degeneration].
    Neuhäuser G
    Hippokrates; 1973 Oct; 44(3):316-8. PubMed ID: 4588328
    [No Abstract]   [Full Text] [Related]  

  • 30. Megalocornea-mental retardation syndrome: an additional case.
    Antiñolo G; Rufo M; Borrego S; Morales C
    Am J Med Genet; 1994 Aug; 52(2):196-7. PubMed ID: 7802008
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cohen syndrome.
    Alavi S; Kher A; Kumar A; Muranjan M; Bharucha B
    Indian Pediatr; 1993 May; 30(5):678-81. PubMed ID: 8282400
    [No Abstract]   [Full Text] [Related]  

  • 32. Aminopterin Syndrome Sine Aminopterin (ASSA) syndrome in two siblings: further delineation of the syndrome and review of the literature.
    Krajewska-Walasek M
    Genet Couns; 1994; 5(4):345-55. PubMed ID: 7888136
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A familial syndrome with hypotonia, mental retardation and dysmorphic features resembling Cohen syndrome.
    Mejía-Baltodano G; Bobadilla L; Solís A; Mendoza R; Díaz-Gallardo MY; Barros-Núñez P
    Genet Couns; 1997; 8(4):311-6. PubMed ID: 9457500
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Fountain syndrome: further delineation of the clinical syndrome and follow-up data.
    Van Buggenhout GJ; Van Ravenswaaij-Arts CM; Renier WO; Van de Wiel MP; Trommelen JC; Pijkels E; Hamel BC; Fryns JP
    Genet Couns; 1996; 7(3):177-86. PubMed ID: 8897038
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [A child with Zellweger's cerebrohepatorenal syndrome].
    Govaerts L; Corstiaensen J; Bakkeren J; Trujbels F; Monnens L
    Tijdschr Kindergeneeskd; 1983 Apr; 51(2):65-7. PubMed ID: 6879587
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Pallister-Killian and Fryns syndromes.
    Stratton RF; Moore CM; Popham CS; DuPont BR; Mattern VL
    Am J Med Genet; 1994 May; 51(1):90. PubMed ID: 8030681
    [No Abstract]   [Full Text] [Related]  

  • 37. Partial duplication of 4q12q13 leads to a mild phenotype.
    Shashi V; Berry MN; Santos C; Pettenati MJ
    Am J Med Genet; 1999 Sep; 86(1):51-3. PubMed ID: 10440828
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ring chromosome 5 associated with severe growth retardation as the sole major physical abnormality.
    Migliori MV; Cherubini V; Bartolotta E; Pettinari A; Pecora R
    Am J Med Genet; 1994 Jan; 49(1):108-10. PubMed ID: 8172236
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A case with 47,XXY,del(11)(q23) karotype-coexistence of Jacobsen and Klinefelter syndromes.
    Matheisel A; Babinska M; Wierzba J; Wozniak A; Nedoszytko B; Balcerska A; Limon J
    Genet Couns; 2000; 11(3):267-71. PubMed ID: 11043435
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Wolf syndrome. Apropos of 2 cases].
    García González P; Pedraz García C; Merino Marcos L; Salazar Veloz J; Escudero Bueno G; Salazar Villalobos V
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.