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 *

85 related articles for article (PubMed ID: 1929019)

  • 1. [Macrocephaly and multiple hemangiomas in two brothers].
    Martinón Sánchez F; Pérez Gómez E; García Rodríguez JL
    An Esp Pediatr; 1991 Jun; 34(6):475-6. PubMed ID: 1929019
    [No Abstract]   [Full Text] [Related]  

  • 2. Slowly progressive macrocephaly with hamartomas: a new syndrome?
    Halal F; Silver K
    Am J Med Genet; 1989 Jun; 33(2):182-5. PubMed ID: 2764028
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Macrocephaly with hamartomas: Bannayan-Zonana syndrome.
    Miles JH; Zonana J; Mcfarlane J; Aleck KA; Bawle E
    Am J Med Genet; 1984 Oct; 19(2):225-34. PubMed ID: 6507473
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multiple hamartoma syndrome (Cowden disease).
    Gentry WC; Eskritt NR; Gorlin RJ
    Arch Dermatol; 1974 Apr; 109(4):521-5. PubMed ID: 4819107
    [No Abstract]   [Full Text] [Related]  

  • 5. Familial vascular malformations. Report of 25 members of one family.
    Pasyk KA; Argenta LC; Erickson RP
    Clin Genet; 1984 Sep; 26(3):221-7. PubMed ID: 6478643
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multiple hamartoma syndrome (Cowden's disease).
    Weary PE; Gorlin RJ; Gentry WC; Comer JE; Greer KE
    Arch Dermatol; 1972 Nov; 106(5):682-90. PubMed ID: 4635800
    [No Abstract]   [Full Text] [Related]  

  • 7. The Meckel syndrome.
    Verma IC; Srivastava AR; Guha DK
    Indian Pediatr; 1974 Jan; 11(1):79-81. PubMed ID: 4839586
    [No Abstract]   [Full Text] [Related]  

  • 8. Varadi syndrome or Opitz trigonocephaly: overlapping manifestation in two cousins.
    Bankier A; Rose CM
    Am J Med Genet; 1994 Oct; 53(1):85-8. PubMed ID: 7802045
    [No Abstract]   [Full Text] [Related]  

  • 9. [Sarcomatous degeneration of a familial cavernous angiomatosis (Bean's syndrome) (author's transl)].
    Sarrat L; Sarrat P
    Ann Dermatol Venereol; 1980 Apr; 107(4):259-65. PubMed ID: 7189993
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Acrocallosal syndrome in two African brothers born to consanguineous parents.
    Christianson AL; Venter PA; Du Toit JL; Shipalana N; Gericke GS
    Am J Med Genet; 1994 Jun; 51(2):98-101. PubMed ID: 8092201
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The CFC syndrome--report of the first two cases outside the United States.
    Neri G; Sabatino G; Bertini E; Genuardi M
    Am J Med Genet; 1987 Aug; 27(4):767-71. PubMed ID: 3425595
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance.
    Koiffmann CP; Wajntal A; Huyke BJ; Castro RM
    Am J Med Genet; 1988 Feb; 29(2):263-8. PubMed ID: 3354597
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Syndrome identification case report 89: thickened subcutaneous tissue, coarse facies, macrocephaly, and hypotonia.
    Hillig U
    J Clin Dysmorphol; 1983; 1(1):9-12. PubMed ID: 6580387
    [No Abstract]   [Full Text] [Related]  

  • 14. [Blue rubber bleb nevus].
    Jumbou O; Bureau B; Fleischmann M; Litoux P; Stalder JF
    Ann Dermatol Venereol; 1993; 120(3):241-3. PubMed ID: 8239366
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The adducted thumbs syndrome. An autosomal recessive disease with arthrogryposis, dysmyelination, craniostenosis, and cleft palate.
    Christian JC; Andrews PA; Conneally PM; Muller J
    Clin Genet; 1971; 2(2):95-103. PubMed ID: 5116596
    [No Abstract]   [Full Text] [Related]  

  • 16. [Skin hemangiomas in children].
    Huffstadt AJ
    Ned Tijdschr Geneeskd; 1970 Jan; 114(5):181-5. PubMed ID: 5414182
    [No Abstract]   [Full Text] [Related]  

  • 17. [Grieg's cephalopolysyndactylia syndrome in one family].
    Dadali EL
    Klin Med (Mosk); 1987 Jun; 65(6):129-31. PubMed ID: 3041101
    [No Abstract]   [Full Text] [Related]  

  • 18. New autosomal dominant syndrome resembling craniofrontonasal dysplasia.
    Teebi AS
    Am J Med Genet; 1987 Nov; 28(3):581-91. PubMed ID: 3425628
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Greig cephalopolysyndactyly syndrome: report of a family and review of the literature.
    Gollop TR; Fontes LR
    Am J Med Genet; 1985 Sep; 22(1):59-68. PubMed ID: 3901752
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genetic aspects of blue rubber-bleb nevus syndrome and multiple generalized glomangiomatosis].
    Gilardi S; Harms M
    Hautarzt; 1982 Feb; 33(2):96-100. PubMed ID: 6281216
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.