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9. Provisionally unique syndrome of ocular and ectodermal defects in two unrelated boys. Toriello HV; Lacassie Y; Droste P; Higgins JV Am J Med Genet; 1993 Mar; 45(6):764-6. PubMed ID: 8456858 [No Abstract] [Full Text] [Related]
10. [A new case of Weaver's syndrome observed in the neonatal period]. Di Comite A; Saracino P; Tonti R; De Vita L Pediatria (Napoli); 1983; 91(4):435-9. PubMed ID: 6545407 [No Abstract] [Full Text] [Related]
12. Bitemporal aplasia cutis congenita. Vázquez Botet M; Caban F P R Health Sci J; 1989 Aug; 8(2):259-61. PubMed ID: 2616724 [No Abstract] [Full Text] [Related]
13. Lacrimal surgery in patients with congenital cranial or facial anomalies. Hicks C; Pitts J; Rose GE Eye (Lond); 1994; 8 ( Pt 5)():583-91. PubMed ID: 7835458 [TBL] [Abstract][Full Text] [Related]
14. Cranioectodermal dysplasia (Sensenbrenner's syndrome). Young ID J Med Genet; 1989 Jun; 26(6):393-6. PubMed ID: 2661822 [No Abstract] [Full Text] [Related]
15. Craniofacial bony defect with developmental abnormality of facial bones, dental malalignment and ectopic neural tissue in the internal auditory meati--a new syndrome? Colleran GC; Hayes R; Kearns G; Kavanagh P; Moylett E; Lynch SA Eur J Med Genet; 2014; 57(6):302-5. PubMed ID: 24705061 [TBL] [Abstract][Full Text] [Related]
16. A syndrome of facial dysmorphia, birth defects, myelodysplasia and immunodeficiency in three sibs of consanguineous parents. Stoll C; Alembik Y; Lutz P Genet Couns; 1994; 5(2):161-5. PubMed ID: 7917125 [TBL] [Abstract][Full Text] [Related]