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 *

155 related articles for article (PubMed ID: 2569826)

  • 21. [Cryptorchidism with didymo-epididymal dissociation and Robinow's syndrome: 2 case reports].
    Fabbro MA; D'Agostino S; Costa L; Musi L; Cappellari F
    Pediatr Med Chir; 1997; 19(2):121-4. PubMed ID: 9312747
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Melnick-Needles syndrome: indication for an autosomal recessive form.
    ter Haar B; Hamel B; Hendriks J; de Jager J
    Am J Med Genet; 1982 Dec; 13(4):469-77. PubMed ID: 7158646
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A new syndrome associated with absence of lower lid lacrimal punctum, ptosis, elevation deficiency of both eyes and mild facial dysmorphism.
    Guran S; Torun D; Mutlu FM; Uysal Y; Ugurel MS; Bahce M
    Ophthalmic Genet; 2009 Sep; 30(3):146-51. PubMed ID: 19941420
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mentally retarded siblings with congenital heart defect, peculiar facies and cryptorchidism in the male: possible McDonough syndrome with coincidental (X; 20) translocation.
    García-Sagredo JM; Lozano C; Ferrando P; San Román C
    Clin Genet; 1984 Aug; 26(2):117-24. PubMed ID: 6147215
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Ectodermal dysplasia syndrome with eyebrow alopecia, ptosis, strabismus, nystagmus, joint laxity, cerebellar ataxia, and osteopenia.
    Zannolli R; Inchingolo G; Serracca L; Miracco C; De Santi MM; Malandrini A; Biagioli M; Perotti R; Baldi C; Nuti D; Polito E; Gonnelli S
    Am J Med Genet; 2002 Nov; 113(1):111-3. PubMed ID: 12400077
    [No Abstract]   [Full Text] [Related]  

  • 26. [Congenital blepharophimosis, ptosis and epicanthus inversus in a Balinese (Indonesia) family].
    Ney R; Breguet G
    Rev Med Suisse Romande; 1981 Apr; 101(4):269-72. PubMed ID: 7256058
    [No Abstract]   [Full Text] [Related]  

  • 27. Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder.
    Cantú JM; Rivera H; Nazará Z; Rojas Q; Hernández A; García-Cruz D
    Clin Genet; 1980 Sep; 18(3):153-9. PubMed ID: 7192193
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Dominantly inherited ptosis, strabismus and ectopic pupils.
    McPherson E; Robertson C; Cammarano A; Hall JG
    Clin Genet; 1976 Jul; 10(1):21-6. PubMed ID: 949861
    [No Abstract]   [Full Text] [Related]  

  • 30. Goldberg-Shprintzen syndrome: Hirschsprung disease, hypotonia, and ptosis in sibs.
    Yomo A; Taira T; Kondo I
    Am J Med Genet; 1991 Nov; 41(2):188-91. PubMed ID: 1785632
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Newly recognized autosomal recessive faciothoracoskeletal syndrome.
    Richieri-Costa A; Guion-Almeida ML; Lauris JR; Ferreira DM
    Am J Med Genet; 1994 Jan; 49(2):224-8. PubMed ID: 8116673
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Congenital ptosis and blepharophimosis in a mentally retarded girl: a new case of Ohdo syndrome?
    Rasmussen M; Strømme P
    Clin Dysmorphol; 1998 Jan; 7(1):61-3. PubMed ID: 9546834
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Vertical transmission of the Ohdo blepharophimosis syndrome.
    Mhanni AA; Dawson AJ; Chudley AE
    Am J Med Genet; 1998 May; 77(2):144-8. PubMed ID: 9605288
    [TBL] [Abstract][Full Text] [Related]  

  • 34. PHAVER syndrome: an autosomal recessive syndrome of limb pterygia, congenital heart anomalies, vertebral defects, ear anomalies, and radial defects.
    Powell CM; Chandra RS; Saal HM
    Am J Med Genet; 1993 Nov; 47(6):807-11. PubMed ID: 8279476
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Facio-thoraco-genital syndrome: a newly recognized birth defect syndrome.
    Wilf-Miron R; Goodman RM
    J Craniofac Genet Dev Biol; 1987; 7(1):19-22. PubMed ID: 3597718
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [A contribution on Crouzon's disease].
    Pittke EC
    Klin Monbl Augenheilkd; 1983 Aug; 183(2):122-7. PubMed ID: 6632678
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Autosomal dominant inheritance of the Kabuki make-up (Niikawa-Kuroki) syndrome.
    Halal F; Gledhill R; Dudkiewicz A
    Am J Med Genet; 1989 Jul; 33(3):376-81. PubMed ID: 2801772
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome?
    Teebi AS; Kaurah P
    Am J Med Genet; 1996 Dec; 66(3):257-60. PubMed ID: 8985482
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Anterior segment anomalies of the eye associated with multiple skeletal abnormalities and early lethality: confirmation of an autosomal recessive syndrome.
    al-Gazali LI; Bakir M; Sadaghatian MR; Nath R; Haas D
    Clin Dysmorphol; 1999 Apr; 8(2):87-92. PubMed ID: 10319196
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
    Morava E; Lefeber DJ; Urban Z; de Meirleir L; Meinecke P; Gillessen Kaesbach G; Sykut-Cegielska J; Adamowicz M; Salafsky I; Ranells J; Lemyre E; van Reeuwijk J; Brunner HG; Wevers RA
    Eur J Hum Genet; 2008 Jan; 16(1):28-35. PubMed ID: 17971833
    [TBL] [Abstract][Full Text] [Related]  

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