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.
201 related articles for article (PubMed ID: 9457496)
1. A new type of maxillofacial dysostosis, inherited as an X-linked or autosomal recessive trait. Ensink RJ; Brunner HG; Cremers CW Genet Couns; 1997; 8(4):285-90. PubMed ID: 9457496 [TBL] [Abstract][Full Text] [Related]
2. X-linked syndrome of branchial arch and other defects. Toriello HV; Higgins JV; Abrahamson J; Waterman DF; Moore WD Am J Med Genet; 1985 May; 21(1):137-42. PubMed ID: 4039890 [TBL] [Abstract][Full Text] [Related]
3. Mandibulofacial dysostosis, microcephaly and thorax deformities in two brothers: a new recessive syndrome? Delb W; Lipfert S; Henn W Clin Dysmorphol; 2001 Apr; 10(2):105-9. PubMed ID: 11310989 [TBL] [Abstract][Full Text] [Related]
6. Mandibulofacial dysostosis: report on two Brazilian families suggesting autosomal recessive inheritance. Richieri-Costa A; Bortolozo MA; Lauris JR; Lauris RC; Guion-Almeida ML; Marques D; Moreti D Am J Med Genet; 1993 Jul; 46(6):659-64. PubMed ID: 8362908 [TBL] [Abstract][Full Text] [Related]
7. Fully implantable hearing device as a new treatment of conductive hearing loss in Franceschetti syndrome. Tringali S; Pergola N; Ferber-Viart C; Truy E; Berger P; Dubreuil C Int J Pediatr Otorhinolaryngol; 2008 Apr; 72(4):513-7. PubMed ID: 18261808 [TBL] [Abstract][Full Text] [Related]
8. Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder? Ng D; Hadley DW; Tifft CJ; Biesecker LG Am J Med Genet; 2002 Jul; 110(4):308-14. PubMed ID: 12116202 [TBL] [Abstract][Full Text] [Related]
9. Treacher Collins syndrome: a case review. Jensen-Steed G Adv Neonatal Care; 2011 Dec; 11(6):389-94; quiz 395-6. PubMed ID: 22123469 [TBL] [Abstract][Full Text] [Related]
10. Melnick-Needles syndrome: indication for an autosomal recessive form. ter Haar B; Hamel B; Hendriks J; de Jager J Am J Med Genet; 1982 Dec; 13(4):469-77. PubMed ID: 7158646 [TBL] [Abstract][Full Text] [Related]
11. Autosomal or X-linked recessive syndrome of congenital lymphedema, hypoparathyroidism, nephropathy, prolapsing mitral valve, and brachytelephalangy. Dahlberg PJ; Borer WZ; Newcomer KL; Yutuc WR Am J Med Genet; 1983 Sep; 16(1):99-104. PubMed ID: 6638075 [TBL] [Abstract][Full Text] [Related]
13. Treacher-Collins syndrome. Management of major and minor anomalies of the ear. Marres HA; Cremers CW; Marres EH Rev Laryngol Otol Rhinol (Bord); 1995; 116(2):105-8. PubMed ID: 7569369 [TBL] [Abstract][Full Text] [Related]
14. Roberts syndrome or "X-linked amelia"? Gershoni-Baruch R; Drugan A; Bronshtein M; Zimmer EZ Am J Med Genet; 1990 Dec; 37(4):569-72. PubMed ID: 2260610 [TBL] [Abstract][Full Text] [Related]
17. Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1. Thienpont B; Dimitriadou E; Theodoropoulos K; Breckpot J; Fryssira H; Kitsiou-Tzeli S; Tzoufi M; Vermeesch JR; Syrrou M; Devriendt K Eur J Med Genet; 2009; 52(6):393-7. PubMed ID: 19772953 [TBL] [Abstract][Full Text] [Related]
18. Orofacial features of Treacher Collins syndrome. Martelli-Junior H; Coletta RD; Miranda RT; Barros LM; Swerts MS; Bonan PR Med Oral Patol Oral Cir Bucal; 2009 Jul; 14(7):E344-8. PubMed ID: 19300363 [TBL] [Abstract][Full Text] [Related]
19. Family with branchial arch anomalies, hearing loss, ear and commissural lip pits, and rib anomalies. A new autosomal recessive condition: branchio-oto-costal syndrome? Clementi M; Mammi I; Tenconi R Am J Med Genet; 1997 Jan; 68(1):91-3. PubMed ID: 8986284 [TBL] [Abstract][Full Text] [Related]
20. Omphalocele and multiple severe congenital anomalies associated with osteodysplasty (Melnick-Needles syndrome). von Oeyen P; Holmes LB; Trelstad RL; Griscom NT Am J Med Genet; 1982 Dec; 13(4):453-63. PubMed ID: 7158644 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]