BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 477680)

  • 1. Diaphragmatic hernia in a female newborn with focal dermal hypoplasia and marked asymmetric malformations (Goltz-Gorlin syndrome).
    Kunze J; Heyne K; Wiedemann HR
    Eur J Pediatr; 1979 Jun; 131(3):213-8. PubMed ID: 477680
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Focal dermal hypoplasia. Goltz syndrome].
    Libis AS; Pinto IO; Viégas J
    Med Cutan Ibero Lat Am; 1982; 10(3):191-6. PubMed ID: 6296562
    [No Abstract]   [Full Text] [Related]  

  • 3. Diaphragmatic hernia in the Coffin-Siris syndrome.
    Delvaux V; Moerman P; Fryns JP
    Genet Couns; 1998; 9(1):45-50. PubMed ID: 9555587
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fryns syndrome: a case associated with karyotype XO.
    Dawani NM; Al Madhoob AR; Ali FA; Shabib F
    Ann Saudi Med; 2004; 24(2):129-32. PubMed ID: 15323276
    [No Abstract]   [Full Text] [Related]  

  • 5. The radiological features of Goltz syndrome: focal dermal hypoplasia. A report of two cases.
    Boothroyd AE; Hall CM
    Skeletal Radiol; 1988; 17(7):505-8. PubMed ID: 3201278
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Osteopathia striata: a characteristic roentgen finding in focal dermal hypoplasia (Goltz-Gorlin syndrome)].
    Barthels W; Boepple D; Petzel H
    Radiologe; 1982 Dec; 22(12):562-5. PubMed ID: 7156390
    [No Abstract]   [Full Text] [Related]  

  • 7. [Focal dermal hypoplasia, or the Goltz-Gorlin syndrome].
    van Beek RH; Maaswinkel-Mooy PD
    Tijdschr Kindergeneeskd; 1990 Jun; 58(3):103-4. PubMed ID: 2165282
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Report of a case of Goltz-Gorlin syndrome].
    Rodermund OE; Hausmann D
    Hautarzt; 1977 Jan; 28(1):37-9. PubMed ID: 190190
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fryns syndrome phenotype and trisomy 22.
    Ladonne JM; Gaillard D; Carré-Pigeon F; Gabriel R
    Am J Med Genet; 1996 Jan; 61(1):68-70. PubMed ID: 8741922
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Fryns syndrome: report of the first case in the national literature].
    Rentería-Ibarra M; Frías-Márquez SG; Michel-Aceves RJ; Navarrete-Arellano M
    Bol Med Hosp Infant Mex; 1993 Sep; 50(9):666-70. PubMed ID: 8373549
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Skeletal manifestations in Fryns syndrome.
    Tsukahara M; Sase M; Tateishi H; Saito T; Kato H; Furukawa S
    Am J Med Genet; 1995 Jan; 55(2):217-20. PubMed ID: 7717421
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Focal dermal hypoplasia (Goltz syndrome)].
    Corona-Guerra GX; Ochoa-Apreza M
    Bol Med Hosp Infant Mex; 2018; 75(3):178-182. PubMed ID: 29799531
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fryns syndrome without diaphragmatic hernia. Report on a new case and review of the literature.
    Alessandri L; Brayer C; Attali T; Samperiz S; Tiran-Rajaofera I; Ramful D; Pilorget H
    Genet Couns; 2005; 16(4):363-70. PubMed ID: 16440878
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Goltz-Gorlin syndrome in a male].
    Reber T; Wolters T; Goos M
    Hautarzt; 1987 Apr; 38(4):218-23. PubMed ID: 3597088
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Genetic interpretation of linear skin abnormalities].
    Happle R
    Hautarzt; 1978 Jul; 29(7):357-63. PubMed ID: 567211
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Focal dermal hypoplasia (Goltz syndrome) presenting as a severe fetal malformation syndrome.
    Patel JS; Maher ER; Charles AK
    Clin Dysmorphol; 1997 Jul; 6(3):267-72. PubMed ID: 9220199
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Anterolateral diaphragmatic hernia: is it a Morgagni hernia?
    Steiner Z; Mares AJ
    Eur J Pediatr Surg; 1993 Apr; 3(2):112-4. PubMed ID: 8323917
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Goltz-Gorlin-syndrome].
    Leiber B; Olbrich G
    Monatsschr Kinderheilkd (1902); 1972 Sep; 120(9):395-7. PubMed ID: 5082808
    [No Abstract]   [Full Text] [Related]  

  • 19. Truncus arteriosus and other lethal internal anomalies in Goltz syndrome.
    Han XY; Wu SS; Conway DH; Pawel BR; Punnett HH; Martin RA; de Chadarevian JP
    Am J Med Genet; 2000 Jan; 90(1):45-8. PubMed ID: 10602117
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.
    Cunniff C; Jones KL; Saal HM; Stern HJ
    Pediatrics; 1990 Apr; 85(4):499-504. PubMed ID: 2314962
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.