BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 8652086)

  • 1. Marden-Walker phenotype: a diagnostic dilemma.
    Soekarman D; Volcke P; Legius E; Holvoet M; Fryns JP
    Genet Couns; 1996; 7(1):31-9. PubMed ID: 8652086
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Marden-Walker phenotype: spectrum of variability in three infants.
    Ramer JC; Frankel CA; Ladda RL
    Am J Med Genet; 1993 Feb; 45(3):285-91. PubMed ID: 7679543
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Marden-Walker syndrome: case report, nosologic discussion and aspects of counseling.
    Garavelli L; Donadio A; Banchini G; Magnani C; Magnani C; Calzolari E; Fryns JP
    Genet Couns; 2000; 11(2):111-8. PubMed ID: 10893662
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Marden-Walker syndrome: a case report and a critical review of the literature.
    Williams MS; Josephson KD; Wargowski DS
    Clin Dysmorphol; 1993 Jul; 2(3):211-9. PubMed ID: 7506965
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Probable Marden-Walker syndrome: evidence for autosomal recessive inheritance.
    Temtamy SA; Shoukry AS; Raafat M; Mihareb S
    Birth Defects Orig Artic Ser; 1975; 11(2):104-8. PubMed ID: 1227520
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Marden-Walker syndrome--a case report].
    Dumić M; Rojnić-Putarek N; Skrablin-Kucić S; Matić T; Ille J; Radica A
    Lijec Vjesn; 2009; 131(7-8):203-6. PubMed ID: 19769282
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Marden-Walker syndrome in an adult.
    Kotzot D; Schinzel A
    Clin Dysmorphol; 1995 Jul; 4(3):260-5. PubMed ID: 7551165
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Congenital hydrocephalus in clinical practice: a genetic diagnostic approach.
    Verhagen JM; Schrander-Stumpel CT; Krapels IP; de Die-Smulders CE; van Lint FH; Willekes C; Weber JW; Gavilanes AW; Macville MV; Stegmann AP; Engelen JJ; Bakker J; Vos YJ; Frints SG
    Eur J Med Genet; 2011; 54(6):e542-7. PubMed ID: 21839187
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome?
    Belengeanu V; Rozsnyai K; Farcaş S; Velea I; Fryns JP
    Genet Couns; 2005; 16(2):167-71. PubMed ID: 16080297
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardation.
    Mathieu M; De Broca A; Bony H; Piussan C
    Genet Couns; 1993; 4(4):299-303. PubMed ID: 8110419
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnosis of Van den Ende-Gupta syndrome: Approach to the Marden-Walker-like spectrum of disorders.
    Niederhoffer KY; Fahiminiya S; Eydoux P; Mawson J; Nishimura G; Jerome-Majewska LA; Patel MS
    Am J Med Genet A; 2016 Sep; 170(9):2310-21. PubMed ID: 27375131
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A 2.84 Mb deletion at 21q22.11 in a patient clinically diagnosed with Marden-Walker syndrome.
    Carrascosa-Romero MC; Suela J; Pardal-Fernández JM; Bermejo-Sánchez E; Vidal-Company A; MacDonald A; Tébar-Gil R; Martínez-Fernández ML; Martínez-Frías ML
    Am J Med Genet A; 2013 Sep; 161A(9):2281-90. PubMed ID: 23894067
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [3M syndrome: case history].
    Fehlow P
    Klin Padiatr; 2006; 218(5):287-91. PubMed ID: 16586274
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation.
    Cappon SL; Duncan AM; Khalifa MM
    Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Molecular diagnosis of CHARGE syndrom].
    Pedersen AM; Skovby F
    Ugeskr Laeger; 2007 Jan; 169(5):402-6. PubMed ID: 17280632
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hypospadias as a new congenital anomaly in Bowen-Conradi syndrome.
    Aynaci FM; Mocan H; Erduran E; Gedik Y
    Genet Couns; 1994; 5(4):369-71. PubMed ID: 7888139
    [No Abstract]   [Full Text] [Related]  

  • 19. Brief clinical report and review: the Marden-Walker syndrome.
    Jaatoul NY; Haddad NE; Khoury LA; Afifi AK; Bahuth NB; Deeb ME; Mikati MA; Der Kaloustian VM
    Am J Med Genet; 1982 Mar; 11(3):259-71. PubMed ID: 7081292
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Craniofacial dysmorphism with flexion of the fingers. Marden-Walker syndrome?].
    Kubryk N; Borde M
    Sem Hop; 1982 Nov; 58(41):2405-7. PubMed ID: 6297028
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.