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.
3. [Manifestation of congenital rubella syndrome: clinical and epidemiologic aspects]. Lahbil D, Souldi L, Rais L, Lamari H, El Kettani A, Zaghloul K. Bull Soc Belge Ophtalmol; 2007; (303):13-20. PubMed ID: 17894282 [Abstract] [Full Text] [Related]
4. The CHARGE association in a newborn infant. Akisü M, Ozkinay F, Ozyürek R, Küçüktaş A, Kültürsay N. Turk J Pediatr; 1998; 40(2):283-7. PubMed ID: 9714686 [Abstract] [Full Text] [Related]
6. [Hemifacial microsomia. Description of a case with associated rare multiple visceral anomalies]. Lapetina F, Romano A, Teza F, Piantoni G. Pediatr Med Chir; 1985 Apr; 7(3):467-70. PubMed ID: 3837211 [Abstract] [Full Text] [Related]
7. Ocular manifestations of congenital rubella syndrome in a developing country. Vijayalakshmi P, Kakkar G, Samprathi A, Banushree R. Indian J Ophthalmol; 2002 Dec; 50(4):307-11. PubMed ID: 12532496 [Abstract] [Full Text] [Related]
8. [Congenital rubella syndrome caused patent ductus arteriosus and atrial septal defect in a case]. Wang YM, Huang JW, Xu SM, Cao YC, Xu ZJ, Wang GZ, Gao XL, Zhao YH. Zhonghua Er Ke Za Zhi; 2004 Mar; 42(3):223. PubMed ID: 15144723 [No Abstract] [Full Text] [Related]
12. 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 [Abstract] [Full Text] [Related]
13. Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the disease. Franceschini P, Vardeu MP, Signorile F, Testa A, Guala A, Franceschini D, Dalforno L. Am J Med Genet; 1993 May 15; 46(3):341-4. PubMed ID: 8488882 [Abstract] [Full Text] [Related]
14. [Autosomal dominant Mendelian midline complex. Secundum atrial septal defect associated with cardiac and facial-thoracic defects. A familial case]. Stéphan E, Ashoush R, Mégarbané A, Kassab R, Salem N, Loiselet J, Bouvagnet P. Arch Mal Coeur Vaiss; 2000 May 15; 93(5):641-7. PubMed ID: 10858865 [Abstract] [Full Text] [Related]
15. 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; 15(4):411-21. PubMed ID: 17290277 [Abstract] [Full Text] [Related]
16. Unilateral microtia in an infant with trisomy 18 mosaicism. Giannatou E, Leze H, Katana A, Kolialexi A, Mavrou A, Kanavakis E, Kitsiou-Tzeli S. Genet Couns; 2009 Apr 15; 20(2):181-7. PubMed ID: 19650416 [Abstract] [Full Text] [Related]