111 related articles for article (PubMed ID: 2240024)
1. Rokitansky sequence in association with the facio-auriculo-vertebral sequence: part of a mesodermal malformation spectrum?
Wulfsberg EA; Grigbsy TM
Am J Med Genet; 1990 Sep; 37(1):100-2. PubMed ID: 2240024
[TBL] [Abstract][Full Text] [Related]
2. Facio-auriculo-vertebral sequence in association with DiGeorge sequence, Rokitansky sequence, and Dandy-Walker malformation: case report.
Pillay K; Matthews LS; Wainwright HC
Pediatr Dev Pathol; 2003; 6(4):355-60. PubMed ID: 14692650
[TBL] [Abstract][Full Text] [Related]
3. Horseshoe lung and facio-auriculo-vertebral sequence: a previously unreported association.
D'Alessandro L; Kovesi T; Massoud S; Lougheed J; Hunter A; Reisman J
Pediatr Pulmonol; 2006 Jun; 41(6):592-6. PubMed ID: 16617456
[TBL] [Abstract][Full Text] [Related]
4. Severe axial anomalies in the oculo-auriculo-vertebral (Goldenhar) complex.
Ignacio Rodríguez J; Palacios J; Lapunzina P
Am J Med Genet; 1993 Aug; 47(1):69-74. PubMed ID: 8368256
[TBL] [Abstract][Full Text] [Related]
5. Oculoauriculovertebral spectrum with radial defects: a new syndrome or an extension of the oculoauriculovertebral spectrum? Report of fourteen Brazilian cases and review of the literature.
Vendramini S; Richieri-Costa A; Guion-Almeida ML
Eur J Hum Genet; 2007 Apr; 15(4):411-21. PubMed ID: 17290277
[TBL] [Abstract][Full Text] [Related]
6. Severe axial mesodermal dysplasia spectrum in an infant of a diabetic mother.
Depraetere M; Dehauwere R; Mariën P; Fryns JP
Genet Couns; 1995; 6(4):303-7. PubMed ID: 8775416
[TBL] [Abstract][Full Text] [Related]
7. Bilateral femoral hypoplasia associated with Rokitansky sequence: another example of a mesodermal malformation spectrum?
Bau CH; Ribeiro CA; Ribeiro SA; Flores RZ
Am J Med Genet; 1994 Jan; 49(2):205-6. PubMed ID: 8116669
[TBL] [Abstract][Full Text] [Related]
8. Child with manifestations of Nager acrofacial dysostosis, and the MURCS, VACTERL, and pulmonary agenesis associations: complex defect of blastogenesis?
David A; Mercier J; Verloes A
Am J Med Genet; 1996 Mar; 62(1):1-5. PubMed ID: 8779315
[TBL] [Abstract][Full Text] [Related]
9. [Unilateral agenesis of the ear with facial asymmetry and vertebral anomalies (an incomplete form of oculo-auriculo- vertebral dysplasia)].
Dodinval P; Michiels H
J Genet Hum; 1976 Nov; 24 Suppl():231-41. PubMed ID: 1025276
[No Abstract] [Full Text] [Related]
10. OEIS complex with craniofacial anomalies--defect of blastogenesis?
Haldar A; Sharma AK; Phadke SR; Jain A; Agarwal SS
Am J Med Genet; 1994 Oct; 53(1):21-3. PubMed ID: 7802030
[TBL] [Abstract][Full Text] [Related]
11. [Clinico-epidemiologic study of microtia].
Sánchez O; Méndez JR; Gómez E; Guerra D
Invest Clin; 1997 Dec; 38(4):203-17. PubMed ID: 9527388
[TBL] [Abstract][Full Text] [Related]
12. Congenital abnormalities associated with limb deficiency defects: a population study based on cases from the Hungarian Congenital Malformation Registry (1975-1984).
Evans JA; Vitez M; Czeizel A
Am J Med Genet; 1994 Jan; 49(1):52-66. PubMed ID: 8172251
[TBL] [Abstract][Full Text] [Related]
13. Normal pulmonary function in a monoamniotic twin discordant for bilateral renal agenesis: report and review.
Klinger G; Merlob P; Aloni D; Maayan A; Sirota L
Am J Med Genet; 1997 Nov; 73(1):76-9. PubMed ID: 9375927
[TBL] [Abstract][Full Text] [Related]
14. Familial microtia, meatal atresia, and conductive deafness in three siblings.
Schmid M; Schröder M; Langenbeck U
Am J Med Genet; 1985 Oct; 22(2):327-32. PubMed ID: 4050865
[TBL] [Abstract][Full Text] [Related]
15. Review of the etiologic heterogeneity of the oculo-auriculo-vertebral spectrum (Hemifacial Microsomia).
Hartsfield JK
Orthod Craniofac Res; 2007 Aug; 10(3):121-8. PubMed ID: 17651128
[TBL] [Abstract][Full Text] [Related]
16. Cardio-facio-cutaneous (CFC) syndrome: report of a new patient.
Chrzanowska K; Fryns JP; Van den Berghe H
Am J Med Genet; 1989 Aug; 33(4):471-3. PubMed ID: 2596505
[TBL] [Abstract][Full Text] [Related]
17. Left microtia in one monozygotic twin. A case report.
Neal GS; Hankins GD
J Reprod Med; 1992 Apr; 37(4):375-7. PubMed ID: 1593565
[TBL] [Abstract][Full Text] [Related]
18. Axial mesodermal dysplasia sequence: autopsy findings.
Merchant SN; Naimi TS; Khan A; Nadol JB; Holmes LB
Clin Dysmorphol; 2004 Jan; 13(1):21-4. PubMed ID: 15127759
[TBL] [Abstract][Full Text] [Related]
19. Two cases of the caudal duplication anomaly including a discordant monozygotic twin.
Kroes HY; Takahashi M; Zijlstra RJ; Baert JA; Kooi KA; Hofstra RM; van Essen AJ
Am J Med Genet; 2002 Nov; 112(4):390-3. PubMed ID: 12376942
[TBL] [Abstract][Full Text] [Related]
20. Interrelationships of the hemifacial microsomia-VATER, VATER, and sirenomelia phenotypes.
Duncan PA; Shapiro LR
Am J Med Genet; 1993 Aug; 47(1):75-84. PubMed ID: 8368258
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]