146 related articles for article (PubMed ID: 11450388)
1. Roberts-SC phocomelia syndrome.
Maheshwari A; Kumar P; Dutta S; Narang A
Indian J Pediatr; 2001 Jun; 68(6):557-9. PubMed ID: 11450388
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [Roberts-SC phocomelia syndrome].
Musfeld DA; Bühler EM; Heinzl S
Gynakol Geburtshilfliche Rundsch; 2001; 41(1):3-7. PubMed ID: 11423730
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. The importance of chromosome studies in Roberts syndrome/SC phocomelia and other cohesinopathies.
Gerkes EH; van der Kevie-Kersemaekers AM; Yakin M; Smeets DF; van Ravenswaaij-Arts CM
Eur J Med Genet; 2010; 53(1):40-4. PubMed ID: 19878742
[TBL] [Abstract][Full Text] [Related]
6. Roberts syndrome: study of 4 new Rgyptian cases with comparison of clinical and cytogenetic findings.
Temtamy SA; Ismail S; Helmy NA
Genet Couns; 2006; 17(1):1-13. PubMed ID: 16719272
[TBL] [Abstract][Full Text] [Related]
7. Cytogenetic findings in Roberts-SC phocomelia syndrome(s).
Tomkins D; Hunter A; Roberts M
Am J Med Genet; 1979; 4(1):17-26. PubMed ID: 495649
[TBL] [Abstract][Full Text] [Related]
8. [Roberts-SC phocomelia syndrome].
Kawame H
Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):234-5. PubMed ID: 11057210
[No Abstract] [Full Text] [Related]
9. The Roberts syndrome/SC phocomelia spectrum--a case report of an adult with review of the literature.
Goh ES; Li C; Horsburgh S; Kasai Y; Kolomietz E; Morel CF
Am J Med Genet A; 2010 Feb; 152A(2):472-8. PubMed ID: 20101700
[TBL] [Abstract][Full Text] [Related]
10. Roberts-SC phocomelia syndrome: a case with additional anomalies.
Satar M; Atici A; Bişak U; Tunali N
Clin Genet; 1994 Feb; 45(2):107-8. PubMed ID: 8004795
[TBL] [Abstract][Full Text] [Related]
11. Tetra-amelia and splenogonadal fusion in Roberts syndrome.
de Ravel TJ; Seftel MD; Wright CA
Am J Med Genet; 1997 Jan; 68(2):185-9. PubMed ID: 9028456
[TBL] [Abstract][Full Text] [Related]
12. A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance.
Fryns JP; Moerman P
Genet Couns; 1998; 9(1):61-2. PubMed ID: 9555592
[No Abstract] [Full Text] [Related]
13. 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]
14. [Roberts-SC phocomelia syndrome: cytogenetic findings and clinical variability in three brothers].
Antiñolo Gil G; Borrego López S; Cañadas García de León M; Sánchez García J
An Esp Pediatr; 1988 Sep; 29(3):239-43. PubMed ID: 3057982
[TBL] [Abstract][Full Text] [Related]
15. Roberts'--SC phocomelia syndrome with cytogenetic findings.
Leonard P; Rendle-Short J; Skardoon L
Hum Genet; 1982; 60(4):379-80. PubMed ID: 7106776
[No Abstract] [Full Text] [Related]
16. 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]
17. [A fatal autosomal recessive syndrome with multiple congenital contractures].
Herva R; Leisti J; Kirkinen P; Seppänen U; Martikainen J
Duodecim; 1985; 101(8):756-62. PubMed ID: 4039655
[No Abstract] [Full Text] [Related]
18. A sibship with Roberts/SC phocomelia syndrome.
Holmes-Siedle M; Seres-Santamaria A; Crocker M; Hall JG; Crouchman M
Am J Med Genet; 1990 Sep; 37(1):18-22. PubMed ID: 2240038
[TBL] [Abstract][Full Text] [Related]
19. [Genetic morphological fatal syndromes. The Fryns syndrome].
Henkel KE; Pfeiffer RA; Stöss H
Pathologe; 1993 Mar; 14(2):92-3. PubMed ID: 8469652
[No Abstract] [Full Text] [Related]
20. Prenatal diagnosis of Roberts syndrome: two new cases.
Benzacken B; Savary JB; Manouvrier S; Bucourt M; Gonzales J
Prenat Diagn; 1996 Feb; 16(2):125-30. PubMed ID: 8650122
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
