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.
151 related articles for article (PubMed ID: 9129742)
1. The Marshall syndrome: report of a new family and review of the literature. Shanske AL; Bogdanow A; Shprintzen RJ; Marion RW Am J Med Genet; 1997 May; 70(1):52-7. PubMed ID: 9129742 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Marshall syndrome: further evidence of a distinct phenotypic entity and report of new findings. Khalifa O; Imtiaz F; Ramzan K; Allam R; Hemidan AA; Faqeih E; Abuharb G; Balobaid A; Sakati N; Owain MA Am J Med Genet A; 2014 Oct; 164A(10):2601-6. PubMed ID: 25073711 [TBL] [Abstract][Full Text] [Related]
4. [Marshall syndrome: Clinical, radiological and genetical features of a Tunisian family]. Sakka R; Kerkeni E; Chaabouni M; Chioukh FZ; Ben Amor S; M'rad R; Ben Yahia S; Chaabouni H; Monastiri K Tunis Med; 2015 Mar; 93(3):170-4. PubMed ID: 26367406 [TBL] [Abstract][Full Text] [Related]
5. Branchio-oculo-facial syndrome and branchio-otic/branchio-oto-renal syndromes are distinct entities. Trummer T; Müller D; Schulze A; Vogel W; Just W J Med Genet; 2002 Jan; 39(1):71-3. PubMed ID: 11826031 [No Abstract] [Full Text] [Related]
6. Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes. Annunen S; Körkkö J; Czarny M; Warman ML; Brunner HG; Kääriäinen H; Mulliken JB; Tranebjaerg L; Brooks DG; Cox GF; Cruysberg JR; Curtis MA; Davenport SL; Friedrich CA; Kaitila I; Krawczynski MR; Latos-Bielenska A; Mukai S; Olsen BR; Shinno N; Somer M; Vikkula M; Zlotogora J; Prockop DJ; Ala-Kokko L Am J Hum Genet; 1999 Oct; 65(4):974-83. PubMed ID: 10486316 [TBL] [Abstract][Full Text] [Related]
7. Audiovestibular phenotype associated with a COL11A1 mutation in Marshall syndrome. Griffith AJ; Gebarski SS; Shepard NT; Kileny PR Arch Otolaryngol Head Neck Surg; 2000 Jul; 126(7):891-4. PubMed ID: 10889003 [TBL] [Abstract][Full Text] [Related]
8. Genetics and hearing loss: a review of Stickler syndrome. Nowak CB J Commun Disord; 1998; 31(5):437-53; 453-4. PubMed ID: 9777489 [TBL] [Abstract][Full Text] [Related]
9. A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndrome. Stoll C; Terzic J; Fischbach M Genet Couns; 1999; 10(4):337-43. PubMed ID: 10631920 [TBL] [Abstract][Full Text] [Related]
12. [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]
13. A novel mutation in ACTG1 causing Baraitser-Winter syndrome with extremely variable expressivity in three generations. Kemerley A; Sloan C; Pfeifer W; Smith R; Drack A Ophthalmic Genet; 2017; 38(2):152-156. PubMed ID: 27096712 [TBL] [Abstract][Full Text] [Related]
14. Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss: a possible new genetic syndrome. Cunningham ET; Eliott D; Miller NR; Maumenee IH; Green WR Arch Ophthalmol; 1998 Jan; 116(1):78-82. PubMed ID: 9445211 [TBL] [Abstract][Full Text] [Related]
15. Daughter and her mildly affected father with Keipert syndrome. Dumic M; Kokic DD; Matic T; Potocki K Am J Med Genet A; 2006 Nov; 140(22):2488-92. PubMed ID: 17036315 [TBL] [Abstract][Full Text] [Related]
16. Oto- spondylo-megaepiphyseal dysplasia (OSMED): clinical description of three patients homozygous for a missense mutation in the COL11A2 gene. van Steensel MA; Buma P; de Waal Malefijt MC; van den Hoogen FH; Brunner HG Am J Med Genet; 1997 Jun; 70(3):315-23. PubMed ID: 9188673 [TBL] [Abstract][Full Text] [Related]
17. COL11A2 mutation associated with autosomal recessive Weissenbacher-Zweymuller syndrome: molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED). Harel T; Rabinowitz R; Hendler N; Galil A; Flusser H; Chemke J; Gradstein L; Lifshitz T; Ofir R; Elbedour K; Birk OS Am J Med Genet A; 2005 Jan; 132A(1):33-5. PubMed ID: 15558753 [TBL] [Abstract][Full Text] [Related]
18. Sensenbrenner syndrome: a new member of the hepatorenal fibrocystic family. Zaffanello M; Diomedi-Camassei F; Melzi ML; Torre G; Callea F; Emma F Am J Med Genet A; 2006 Nov; 140(21):2336-40. PubMed ID: 17022080 [TBL] [Abstract][Full Text] [Related]
19. 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]