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 *

132 related articles for article (PubMed ID: 6638067)

  • 1. AREDYLD: a syndrome combining an acrorenal field defect, ectodermal dysplasia, lipoatrophic diabetes, and other manifestations.
    Pinheiro M; Freire-Maia N; Chautard-Freire-Maia EA; Araujo LM; Liberman B
    Am J Med Genet; 1983 Sep; 16(1):29-33. PubMed ID: 6638067
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An autosomal recessive ectodermal dysplasia syndrome of hypotrichosis, onychodysplasia, hyperkeratosis, kyphoscoliosis, catartact, and other manifestations.
    Alves AF; dos Santos PA; Castelo-Branco-Neto E; Freire-Maia N
    Am J Med Genet; 1981; 10(3):213-8. PubMed ID: 7304669
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autosomal recessive cleft lip/palate, ectodermal dysplasia, and minor acral anomalies: report of a Brazilian family.
    Richieri-Costa A; Guion-Almeida ML; Freire-Maia N; Pinheiro M
    Am J Med Genet; 1992 Sep; 44(2):158-62. PubMed ID: 1456284
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ectodermal dysplasia, lipoatrophy, diabetes mellitus, and amastia: a second case of the AREDYLD syndrome.
    Breslau-Siderius EJ; Toonstra J; Baart JA; Koppeschaar HP; Maassen JA; Beemer FA
    Am J Med Genet; 1992 Oct; 44(3):374-7. PubMed ID: 1488989
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cleft lip/palate-oligodontia-syndactyly-hair alterations, a new syndrome: review of the conditions combining ectodermal dysplasia and cleft lip/palate.
    Martínez B; Monasterio L; Pinheiro M; Freire-Maia N
    Am J Med Genet; 1987 May; 27(1):23-31. PubMed ID: 3037904
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Pigmentosum retinis and tubulo-interstitial nephronophtisis in Sensenbrenner syndrome: a case report].
    Costet C; Betis F; Bérard E; Tsimaratos M; Sigaudy S; Antignac C; Gastaud P
    J Fr Ophtalmol; 2000 Feb; 23(2):158-60. PubMed ID: 10705117
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Autosomal recessive ectodermal dysplasia: I. An undescribed dysplasia/malformation syndrome.
    Bustos T; Simosa V; Pinto-Cisternas J; Abramovits W; Jolay L; Rodriguez L; Fernandez L; Ramela M
    Am J Med Genet; 1991 Dec; 41(4):398-404. PubMed ID: 1776626
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child.
    Moerman P; Fryns JP
    Am J Med Genet; 1996 Jun; 63(3):479-81. PubMed ID: 8737656
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [AREDYLD syndrome].
    Masuno M
    Ryoikibetsu Shokogun Shirizu; 2001; (33):218. PubMed ID: 11462408
    [No Abstract]   [Full Text] [Related]  

  • 10. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG; Reed SD; Rosenbaum KN; Gershanik J; Chen H; Wilson KM
    Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A previously undescribed ectodermal dysplasia of the tricho-odonto-onychial subgroup in a family.
    Tsakalakos N; Jordaan FH; Taljaard JJ; Hough SF
    Arch Dermatol; 1986 Sep; 122(9):1047-53. PubMed ID: 3740884
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Trichoodontoonychial dysplasia--a new meso-ectodermal dysplasia.
    Pinheiro M; Freire-Maia N; Roth AJ
    Am J Med Genet; 1983 May; 15(1):67-70. PubMed ID: 6859125
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Odontoonychodysplasia with alopecia: a new pure ectodermal dysplasia with probable autosomal recessive inheritance.
    Pinheiro M; Freire-Maia N; Gollop TR
    Am J Med Genet; 1985 Jan; 20(1):197-202. PubMed ID: 2982262
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Arthrogryposis, ectodermal dysplasia and other anomalies in two sisters.
    Stoll C; Alembik Y; Finck S; Janser B
    Genet Couns; 1992; 3(1):35-9. PubMed ID: 1590979
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cataracts, alopecia, and sclerodactyly: a previously apparently undescribed ectodermal dysplasia syndrome on the island of Rodrigues.
    Wallis C; Ip FS; Beighton P
    Am J Med Genet; 1989 Apr; 32(4):500-3. PubMed ID: 2773993
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A Rapp-Hodgkin like syndrome in three sibs: clinical, dental and dermatoglyphic study.
    Atasu M; Akesi S; Elçioglu N; Yatmaz PI; Ertas EB
    Clin Dysmorphol; 1999 Apr; 8(2):101-10. PubMed ID: 10319198
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new autosomal recessive disorder resembling Weaver syndrome.
    Teebi AS; Sundareshan TS; Hammouri MY; al-Awadi SA; al-Saleh QA
    Am J Med Genet; 1989 Aug; 33(4):479-82. PubMed ID: 2596508
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mental retardation, hypotrichosis and syndactyly: a new entity?
    Lopes VL; Marques-De-Faria AP
    Genet Couns; 1996; 7(1):47-51. PubMed ID: 8652088
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Scalp-ear-nipple syndrome: additional manifestations.
    Edwards MJ; McDonald D; Moore P; Rae J
    Am J Med Genet; 1994 Apr; 50(3):247-50. PubMed ID: 8042668
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?
    Janssen HC; Schaap C; Vandevijver N; Moerman P; de Die-Smulders CE; Fryns JP
    J Med Genet; 1999 Jun; 36(6):481-4. PubMed ID: 10874639
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.