168 related articles for article (PubMed ID: 6650564)
1. The Weissenbacher-Zweymüller, Stickler, and Marshall syndromes: further evidence for their identity.
Winter RM; Baraitser M; Laurence KM; Donnai D; Hall CM
Am J Med Genet; 1983 Oct; 16(2):189-99. PubMed ID: 6650564
[TBL] [Abstract][Full Text] [Related]
2. The ocular manifestations of Weissenbacher-Zweymuller syndrome.
Rabinowitz R; Gradstein L; Galil A; Levy J; Lifshitz T
Eye (Lond); 2004 Dec; 18(12):1258-63. PubMed ID: 15044941
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia.
Chemke J; Carmi R; Galil A; Bar-Ziv Y; Ben-Ytzhak I; Zurkowski L
Am J Med Genet; 1992 Aug; 43(6):989-95. PubMed ID: 1415350
[TBL] [Abstract][Full Text] [Related]
5. Marshall-Smith syndrome: two case reports and a review of pulmonary manifestations.
Johnson JP; Carey JC; Glassy FJ; Paglieroni T; Lipson MH
Pediatrics; 1983 Feb; 71(2):219-23. PubMed ID: 6823423
[TBL] [Abstract][Full Text] [Related]
6. [Lens coloboma and lens dislocation in Stickler (Marshall) syndrome].
Schlote T; Völker M; Knorr M; Thiel HJ
Klin Monbl Augenheilkd; 1997 Apr; 210(4):227-8. PubMed ID: 9235398
[TBL] [Abstract][Full Text] [Related]
7. Autosomal recessive deafness with skeletal dysplasia and facial appearance of Marshall syndrome.
Miny P; Lenz W
Am J Med Genet; 1985 Jun; 21(2):317-24. PubMed ID: 4014313
[TBL] [Abstract][Full Text] [Related]
8. Inverted nipples in Robinow syndrome.
Lorenzetti MH; Fryns JP
Genet Couns; 1996; 7(1):67-9. PubMed ID: 8652091
[TBL] [Abstract][Full Text] [Related]
9. Neonatal death in Marshall-Smith syndrome.
Chatel C; Maazoul F; Sigaudy S; Fredouille C; Ayme S; Philip N
Genet Couns; 1998; 9(1):15-8. PubMed ID: 9555581
[TBL] [Abstract][Full Text] [Related]
10. Weissenbacher-Zweymuller syndrome: long-term follow-up of growth and psychomotor development.
Galil A; Carmi R; Goldstein E; Porter B; Bar Ziv J; Chemke J
Dev Med Child Neurol; 1991 Dec; 33(12):1104-9. PubMed ID: 1723388
[TBL] [Abstract][Full Text] [Related]
11. [Clinical and genetic heterogeneity in Robinow's syndrome. Report of a new case and review of the literature I].
Oliván Gonzalvo G; Pérez González JM; Ventura Faci P; Olivares López JL; Bueno Sánchez M
An Esp Pediatr; 1990 Jul; 33(1):76-81. PubMed ID: 2252296
[No Abstract] [Full Text] [Related]
12. A new short rib syndrome: report of two cases.
Beemer FA; Langer LO; Klep-de Pater JM; Hemmes AM; Bylsma JB; Pauli RM; Myers TL; Haws CC
Am J Med Genet; 1983 Jan; 14(1):115-23. PubMed ID: 6829599
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Marshall syndrome.
Stratton RF; Lee B; Ramirez F
Am J Med Genet; 1991 Oct; 41(1):35-8. PubMed ID: 1951461
[TBL] [Abstract][Full Text] [Related]
15. Marshall-Smith syndrome.
Herman TE; Siegel MJ
J Perinatol; 2015 Apr; 35(4):307-9. PubMed ID: 25813678
[No Abstract] [Full Text] [Related]
16. The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.
Dimitrov B; Balikova I; Bradinova I; Zahariev D; Popova A; Simeonov E; De Smet L; Devriendt K; Fryns JP
Genet Couns; 2005; 16(2):181-6. PubMed ID: 16080300
[No Abstract] [Full Text] [Related]
17. Significant ophthalmoarthropathy associated with ectodermal dysplasia in a child with Marshall-Stickler overlap: a case report.
Al Kaissi A; Ganger R; Klaushofer K; Grill F
Cases J; 2008 Oct; 1(1):270. PubMed ID: 18950500
[TBL] [Abstract][Full Text] [Related]
18. Stickler syndrome: report of four cases.
Kulkarni ML; Sureshkumar C; George VG
Ann Dent; 1993; 52(2):23-7. PubMed ID: 8267375
[No Abstract] [Full Text] [Related]
19. Marshall-Smith syndrome: a distinct entity.
Sharma AK; Haldar A; Phadke S; Agarwal SS
Indian Pediatr; 1994 Sep; 31(9):1098-100. PubMed ID: 7883370
[No Abstract] [Full Text] [Related]
20. Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome).
Pihlajamaa T; Prockop DJ; Faber J; Winterpacht A; Zabel B; Giedion A; Wiesbauer P; Spranger J; Ala-Kokko L
Am J Med Genet; 1998 Nov; 80(2):115-20. PubMed ID: 9805126
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
