BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 7536394)

  • 1. Dubowitz syndrome: long-term follow-up of an original patient.
    Hansen KE; Kirkpatrick SJ; Laxova R
    Am J Med Genet; 1995 Jan; 55(2):161-4. PubMed ID: 7536394
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dubowitz syndrome: review of 141 cases including 36 previously unreported patients.
    Tsukahara M; Opitz JM
    Am J Med Genet; 1996 May; 63(1):277-89. PubMed ID: 8723121
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Dubowitz syndrome: a retrospective.
    Moller KT; Gorlin RJ
    J Craniofac Genet Dev Biol Suppl; 1985; 1():283-6. PubMed ID: 3877102
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Dubowitz syndrome.
    Wilroy RS; Tipton RE; Summitt RL
    Am J Med Genet; 1978; 2(3):275-84. PubMed ID: 263660
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Dubowitz syndrome. A diagnosis not to be missed].
    Mathieu M; Berquin P; Epelbaum S; Lenaerts C; Piussan C
    Arch Fr Pediatr; 1991 Dec; 48(10):715-8. PubMed ID: 1793348
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The Dubowitz syndrome].
    Dumić M; Cvitković M; Letinić D; Filipović-Grcić B; Kordić R
    Lijec Vjesn; 1994; 116(5-6):135-7. PubMed ID: 7968200
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New findings in a patient with Dubowitz syndrome: velopharyngeal insufficiency and hypoparathyroidism.
    Lerman-Sagie T; Merlob P; Shuper A; Kauli R; Kozokaro Z; Grunebaum M; Mimouni M
    Am J Med Genet; 1990 Oct; 37(2):241-3. PubMed ID: 2248292
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sudden development of bilateral cataract in a child with Dubowitz syndrome: a case report.
    Annemans I; Foets B; Jaeken J; Casteels I
    Bull Soc Belge Ophtalmol; 2000; (278):23-5. PubMed ID: 11761556
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dubowitz syndrome in a boy without developmental delay: further evidence for phenotypic variability.
    Wallerstein R; Kacmar J; Anderson CE; Jackson L
    Am J Med Genet; 1997 Jan; 68(2):216-8. PubMed ID: 9028461
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Peters'-Plus syndrome: description of 16 patients and review of the literature.
    Hennekam RC; Van Schooneveld MJ; Ardinger HH; Van Den Boogaard MJ; Friedburg D; Rudnik-Schoneborn S; Seguin JH; Weatherstone KB; Wittebol-Post D; Meinecke P
    Clin Dysmorphol; 1993 Oct; 2(4):283-300. PubMed ID: 7508316
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Dubowitz syndrome: further observations.
    Orrison WW; Schnitzler ER; Chun RW
    Am J Med Genet; 1980; 7(2):155-70. PubMed ID: 6258433
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Blepharophimosis, ptosis and mental retardation: further delineation of Ohdo syndrome.
    Melnyk AR
    Clin Dysmorphol; 1994 Apr; 3(2):121-4. PubMed ID: 7519949
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mild growth retardation and developmental delay, microcephaly, and a distinctive facial appearance.
    Partington M; Anderson D
    Am J Med Genet; 1994 Jan; 49(2):247-50. PubMed ID: 7509568
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: a new example of the Chitty syndrome.
    Van Daele SG; Van Coster RN; Meire F; Smets AM; Leroy JG
    Am J Med Genet; 1996 Oct; 65(3):205-8. PubMed ID: 9240744
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Dubowitz syndrome--one more case.
    Chrzanowska KH; Krajewska-Walasek M
    Klin Padiatr; 1987; 199(5):370-2. PubMed ID: 3316825
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
    Hamel BC; Mariman EC; van Beersum SE; Schoonbrood-Lenssen AM; Ropers HH
    Am J Med Genet; 1994 Jul; 51(4):591-7. PubMed ID: 7943045
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Dubowitz syndrome: the psychological status of ten cases at follow-up.
    Parrish JM; Wilroy RS
    Am J Med Genet; 1980; 6(1):3-8. PubMed ID: 7190357
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An exceptional Albanian family with seven children presenting with dysmorphic features and mental retardation: maternal phenylketonuria.
    Knerr I; Zschocke J; Schellmoser S; Topf HG; Weigel C; Dötsch J; Rascher W
    BMC Pediatr; 2005 Apr; 5(1):5. PubMed ID: 15811181
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Kivlin syndrome and Peters'-Plus syndrome: are they the same disorder?
    Thompson EM; Winter RM; Baraitser M
    Clin Dysmorphol; 1993 Oct; 2(4):301-16. PubMed ID: 7508317
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Filippi syndrome: report of three additional cases.
    Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
    Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.