269 related articles for article (PubMed ID: 8650122)
1. 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]
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. The SC phocomelia syndrome: report of two cases with cytogenetic abnormality.
Qazi QH; Kassner EG; Masakawa A; Madahar C; Choi SJ
Am J Med Genet; 1979; 4(3):231-8. PubMed ID: 517578
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. [Roberts' syndrome. Review of the literature and presentation of 2 clinical cases].
Colombo B; Bottelli A; Maserati E
Pediatr Med Chir; 1986; 8(3):411-3. PubMed ID: 3786205
[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. 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]
9. [Pyknodysostosis. Review and report of 6 cases].
Nielsen EL
Ugeskr Laeger; 1973 Sep; 135(39):2093-8. PubMed ID: 4590079
[No Abstract] [Full Text] [Related]
10. Ring chromosome 15 syndrome.
Fryns JP; Jaeken J; Devlieger H; Debucquoy P; Eggermont E; Van den Berghe H
Acta Paediatr Belg; 1981; 34(1):47-9. PubMed ID: 7270144
[No Abstract] [Full Text] [Related]
11. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
Habecker-Green JG; Naeem R; Gold H; O'Grady JP; Kanaan C; Bayer-Zwirello L; Murray MS; Cohn GM
J Perinatol; 1998; 18(5):395-8. PubMed ID: 9766419
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of mosaic tetrasomy 5p.
Park JP; Barefoot KH; Ornvold K; Berg SZ; Dossu JR; Mohandas TK
Prenat Diagn; 2001 May; 21(5):351-3. PubMed ID: 11360274
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of Roberts syndrome and detection of an ESCO2 frameshift mutation in a Pakistani family.
Schulz S; Gerloff C; Ledig S; Langer D; Volleth M; Shirneshan K; Wieacker P
Prenat Diagn; 2008 Jan; 28(1):42-5. PubMed ID: 18186147
[TBL] [Abstract][Full Text] [Related]
14. Expanding the mutation and clinical spectrum of Roberts syndrome.
Afifi HH; Abdel-Salam GM; Eid MM; Tosson AM; Shousha WG; Abdel Azeem AA; Farag MK; Mehrez MI; Gaber KR
Congenit Anom (Kyoto); 2016 Jul; 56(4):154-62. PubMed ID: 26710928
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Incidental detection of premature centromere separation in amniocytes associated with a mild form of Roberts syndrome.
Stanley WS; Pai GS; Horger EO; Yan YS; McNeal KS
Prenat Diagn; 1988 Oct; 8(8):565-9. PubMed ID: 3205861
[TBL] [Abstract][Full Text] [Related]
17. Pycnodysostosis: a case report.
Lentle BC
J Can Assoc Radiol; 1971 Sep; 22(3):210-4. PubMed ID: 5150109
[No Abstract] [Full Text] [Related]
18. [Karyotyping of fetal cells in the prenatal diagnosis in Costa Rica].
Castro Volio I; Escalante López G; Mora Palma H; Guerra Carles D; Sánchez Chaves L; Peña Obando C
Rev Biol Trop; 1995; 43(1-3):31-7. PubMed ID: 8728757
[TBL] [Abstract][Full Text] [Related]
19. LADD syndrome in five members of a three-generation family and prenatal diagnosis.
Francannet C; Vanlieferinghen P; Dechelotte P; Urbain MF; Campagne D; Malpuech G
Genet Couns; 1994; 5(1):85-91. PubMed ID: 8031542
[TBL] [Abstract][Full Text] [Related]
20. [The formation of risk groups and the performance of invasive prenatal diagnosis].
Arbuzova SB; Khlevnaia LA; Kaznacheeva EB; Nikolenko MI
Tsitol Genet; 1995; 29(5):76-81. PubMed ID: 8721851
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
