199 related articles for article (PubMed ID: 7875788)
1. Prenatal diagnosis of Roberts syndrome.
Sharma AK; Jain A; Phadke SR; Srivastava S
Indian Pediatr; 1994 Oct; 31(10):1261-4. PubMed ID: 7875788
[No Abstract] [Full Text] [Related]
2. Prenatal sonographic diagnosis of Pena-Shokeir syndrome type I.
Ochi H; Kobayashi E; Matsubara K; Katayama T; Ito M
Ultrasound Obstet Gynecol; 2001 Jun; 17(6):546-7. PubMed ID: 11422985
[No Abstract] [Full Text] [Related]
3. Prenatal sonographic diagnosis of Larsen syndrome.
Tongsong T; Wanapirak C; Pongsatha S; Sudasana J
J Ultrasound Med; 2000 Jun; 19(6):419-21. PubMed ID: 10841065
[No Abstract] [Full Text] [Related]
4. [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]
5. US case of the day. Pena-Shokeir phenotype.
Horrow MM; Rosenberg HK; Schneider AS; Greenberg CM; Zaeri N
Radiographics; 1995 May; 15(3):726-9. PubMed ID: 7624577
[No Abstract] [Full Text] [Related]
6. Prenatal sonographic features and management of a fetus with Roberts-SC phocomelia syndrome (pseudothalidomide syndrome) and pulmonary hypoplasia.
Sherer DM; Shah YG; Klionsky N; Woods JR
Am J Perinatol; 1991 Jul; 8(4):259-62. PubMed ID: 1741870
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of tetraploidy.
Sagot P; Nomballais MF; David A; Yvinec M; Beaujard MP; Barrière P; Boog G
Fetal Diagn Ther; 1993; 8(3):182-6. PubMed ID: 8240691
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of unilateral tibial hemimelia.
Dreyfus M; Baldauf JJ; Rigaut E; Clavert JM; Gasser B; Ritter J
Ultrasound Obstet Gynecol; 1996 Mar; 7(3):205-7. PubMed ID: 8705415
[TBL] [Abstract][Full Text] [Related]
9. Fetal ultrasonographic detection of hypodontia in the Neu-Laxova syndrome.
Bronshtein M; Blumenfeld I; Cohen I; Blumenfeld Z
J Clin Ultrasound; 1993; 21(9):648-50. PubMed ID: 8227398
[No Abstract] [Full Text] [Related]
10. Early prenatal diagnosis of Meckel syndrome--a case report.
Yu CJ; Chen CP; Jeng CJ; Yang YC
Zhonghua Yi Xue Za Zhi (Taipei); 1990 Jul; 46(1):53-6. PubMed ID: 2176925
[TBL] [Abstract][Full Text] [Related]
11. Prenatal ultrasound diagnosis of Roberts syndrome in a family with negative history.
Paladini D; Palmieri S; Lecora M; Perone L; Di Meglio A; D'Armiento M; Cascioli C; Martinelli P
Ultrasound Obstet Gynecol; 1996 Mar; 7(3):208-10. PubMed ID: 8705416
[TBL] [Abstract][Full Text] [Related]
12. Genetics casebook. Duplication-deletion syndromes.
Day-Salvatore DL; Guzman E; Farren-Chavez D; Sciorra L; Knuppel R
J Perinatol; 1995; 15(4):333-7. PubMed ID: 8558345
[No Abstract] [Full Text] [Related]
13. Prenatal echographic diagnosis of laryngeal atresia as part of a multiple congenital anomalies (MCA) syndrome.
Witters I; Moerman P; Fryns JP
Genet Couns; 2000; 11(3):215-9. PubMed ID: 11043429
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of E trisomy syndrome by fetography.
Ogita S; Hasegawa H; Matsumoto M; Kamei T; Shimamoto T
Obstet Gynecol; 1974 Jun; 43(6):887-92. PubMed ID: 4597791
[No Abstract] [Full Text] [Related]
15. Nuchal thickening in Jacobsen syndrome.
McClelland SM; Smith AP; Smith NC; Gray ES; Diack JS; Dean JC
Ultrasound Obstet Gynecol; 1998 Oct; 12(4):280-2. PubMed ID: 9819862
[TBL] [Abstract][Full Text] [Related]
16. Meckel syndrome: prenatal ultrasonographic diagnosis in two cases showing marked differences in phenotypic expression.
Gallimore AP; Davies PF
Australas Radiol; 1992 Feb; 36(1):62-4. PubMed ID: 1632751
[TBL] [Abstract][Full Text] [Related]
17. Prenatal ultrasonographic findings associated with Jacobsen syndrome.
Wax JR; Smith JF; Floyd RC; Eggleston MK
J Ultrasound Med; 1995 Mar; 14(3):256-8. PubMed ID: 7760474
[No Abstract] [Full Text] [Related]
18. FOUR CASES OF SIRENOMELIA WITH DIFFERENT MANIFESTATION.
Erdogdu E; Arisoy R; Yuksel MA; Cakar E; Uygur LS; Aydin H; Demirci O; Pekin O
Genet Couns; 2015; 26(3):365-8. PubMed ID: 26625671
[No Abstract] [Full Text] [Related]
19. Phocomelia, flexion deformities and absent thumbs: a new hereditary upper limb malformation.
Holmes LB; Borden S
Pediatrics; 1974 Oct; 54(4):461-5. PubMed ID: 4415048
[No Abstract] [Full Text] [Related]
20. Prenatal diagnosis and subsequent management of a fetus with a 46XY r(4)(p15-q35) karyotype.
Sherer DM; Shah YG; Wang N; Metlay LA; Woods JR
Am J Perinatol; 1991 Jan; 8(1):53-5. PubMed ID: 1987971
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
