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.
311 related articles for article (PubMed ID: 11746009)
1. Limb/pelvis hypoplasia/aplasia with skull defect (Schinzel phocomelia): distinctive features and prenatal detection. Olney RS; Hoyme HE; Roche F; Ferguson K; Hintz S; Madan A Am J Med Genet; 2001 Nov; 103(4):295-301. PubMed ID: 11746009 [TBL] [Abstract][Full Text] [Related]
2. Al-Awadi/Raas-Rothschild syndrome in a newborn with additional anomalies. Alp E; Alp H; Atabek ME; Pirgon Ö J Clin Res Pediatr Endocrinol; 2010; 2(1):49-51. PubMed ID: 21274338 [TBL] [Abstract][Full Text] [Related]
3. A report of two cases of Al-Awadi Raas-Rothschild syndrome (AARRS) supporting that "apparent" Phocomelia differentiates AARRS from Schinzel Phocomelia syndrome (SPS). AlQattan MM; AlAbdulkareem I; Ballow M; Al Balwi M Gene; 2013 Sep; 527(1):371-5. PubMed ID: 23727605 [TBL] [Abstract][Full Text] [Related]
4. Phocomelia, oligodactyly, and acrania: the Schinzel-Phocomelia syndrome. Chitayat D; Stalker HJ; Vekemans M; Delneste D; Azouz EM Am J Med Genet; 1993 Feb; 45(3):297-9. PubMed ID: 8123061 [TBL] [Abstract][Full Text] [Related]
5. Limb/pelvis hypoplasia/aplasia with skull defect (Schinzel phocomelia): distinctive features and prenatal detection. Winter R Am J Med Genet; 2002 Sep; 111(4):457; author reply 458. PubMed ID: 12210314 [No Abstract] [Full Text] [Related]
6. Limb/pelvis-hypoplasia/aplasia syndrome (Al-Awadi/Raas-Rothschild syndrome): report of two Italian sibs and further confirmation of autosomal recessive inheritance. Camera G; Ferraiolo G; Leo D; Spaziale A; Pozzolo S J Med Genet; 1993 Jan; 30(1):65-9. PubMed ID: 8423611 [TBL] [Abstract][Full Text] [Related]
7. Phocomelia, ectrodactyly, skull defect and urinary system anomaly: Schinzel-phocomelia syndrome? Evliyaoğlu N; Temoçin AK; Altintaş DU; Duman N; Satar N; Süleymanova D Clin Genet; 1996 Feb; 49(2):70-3. PubMed ID: 8740915 [TBL] [Abstract][Full Text] [Related]
8. A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome. Kantaputra PN; Mundlos S; Sripathomsawat W Am J Med Genet A; 2010 Nov; 152A(11):2832-7. PubMed ID: 20949531 [TBL] [Abstract][Full Text] [Related]
9. Severe case of Al Awadi/Raas-Rothschild syndrome or new, possibly autosomal recessive facio-skeleto-genital syndrome. Mollica F; Mazzone D; Cimino G; Opitz JM Am J Med Genet; 1995 Mar; 56(2):168-72. PubMed ID: 7625440 [TBL] [Abstract][Full Text] [Related]
10. Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome. Woods CG; Stricker S; Seemann P; Stern R; Cox J; Sherridan E; Roberts E; Springell K; Scott S; Karbani G; Sharif SM; Toomes C; Bond J; Kumar D; Al-Gazali L; Mundlos S Am J Hum Genet; 2006 Aug; 79(2):402-8. PubMed ID: 16826533 [TBL] [Abstract][Full Text] [Related]
11. Roberts-SC phocomelia syndrome with exencephaly. Verloes A; Herens C; Van Maldergem L; Retz MC; Dodinval P Ann Genet; 1989; 32(3):169-70. PubMed ID: 2817778 [TBL] [Abstract][Full Text] [Related]
12. Al-Awadi/Raas-Rothschild/Schinzel (AARRS) phocomelia syndrome: case report and developmental field analysis. Subhani M; Akangire G; Kulkarni A; Wilson GN Am J Med Genet A; 2009 Jul; 149A(7):1494-8. PubMed ID: 19530188 [TBL] [Abstract][Full Text] [Related]
13. The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia. Further evidence for autosomal recessive inheritance. Meinecke P; Fryns JP Clin Genet; 1985 Dec; 28(6):516-20. PubMed ID: 4075561 [TBL] [Abstract][Full Text] [Related]
14. Prenatal detection of Roberts-SC phocomelia syndrome: report of 2 sibs with characteristic manifestations. Robins DB; Ladda RL; Thieme GA; Boal DK; Emanuel BS; Zackai EH Am J Med Genet; 1989 Mar; 32(3):390-4. PubMed ID: 2658590 [TBL] [Abstract][Full Text] [Related]
15. The newly recognised limb/pelvis-hypoplasia/aplasia syndrome: report of a Bedouin patient and review. Farag TI; al-Awadi SA; Marafie MJ; Bastaki L; al-Othman SA; Mohammed FM; AlSuliman IS; Murthy DS J Med Genet; 1993 Jan; 30(1):62-4. PubMed ID: 8423610 [TBL] [Abstract][Full Text] [Related]
16. Phocomelia and additional anomalies in two sisters. Schinzel A Hum Genet; 1990 May; 84(6):539-41. PubMed ID: 2338339 [TBL] [Abstract][Full Text] [Related]
17. Diaphragmatic defects, limb deficiencies, and ossification defects of the skull: a distinctive malformation syndrome. Froster UG; Kolditz P; Wisser J; Robbiani MB; Stallmach T; Hebisch G; Huch R; Huch A Am J Med Genet; 1996 Mar; 62(1):48-53. PubMed ID: 8779324 [TBL] [Abstract][Full Text] [Related]
18. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome. Schrander-Stumpel C; de Die-Smulders C; Fryns JP; da Costa J; Bouckaert P Am J Med Genet; 1990 Sep; 37(1):133-5. PubMed ID: 2240030 [TBL] [Abstract][Full Text] [Related]
19. Familial aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits in an inbred Pakistani Muslim family: a possible new autosomal recessive disorder with overlapping manifestations of the syndromes of Fuhrmann, Al-Awadi, and Raas-Rothschild. Kumar D; Duggan MB; Mueller RF; Karbani G Am J Med Genet; 1997 May; 70(2):107-13. PubMed ID: 9128926 [TBL] [Abstract][Full Text] [Related]