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. A case report of Teschler-Nicola/Killian syndrome. Lubinsky M J Clin Dysmorphol; 1983; 1(3):25-7. PubMed ID: 6584559 [No Abstract] [Full Text] [Related]
4. Abnormal hair, craniofacial dysmorphism, and severe mental retardation - a new syndrome? Killian W; Zonana J; Schroer RJ J Clin Dysmorphol; 1983; 1(3):6-13. PubMed ID: 6584560 [No Abstract] [Full Text] [Related]
5. Teschler-Nicola/Killian syndrome: a case report. Hersh JH; Graham JM; Destrempes MM; Greenstein RM J Clin Dysmorphol; 1983; 1(3):20-4. PubMed ID: 6584558 [No Abstract] [Full Text] [Related]
6. Teschler-Nicola/Killian syndrome: a sporadic case in an 11-year-old male. Hall BD J Clin Dysmorphol; 1983; 1(3):14-7. PubMed ID: 6584555 [No Abstract] [Full Text] [Related]
7. The CFC syndrome--report of the first two cases outside the United States. Neri G; Sabatino G; Bertini E; Genuardi M Am J Med Genet; 1987 Aug; 27(4):767-71. PubMed ID: 3425595 [TBL] [Abstract][Full Text] [Related]
8. Costello syndrome: the natural history of a true postnatal growth retardation syndrome. Umans S; Decock P; Fryns JP Genet Couns; 1995; 6(2):121-5. PubMed ID: 7546454 [TBL] [Abstract][Full Text] [Related]
9. [New hereditary syndrome with mental retardation]. Marincheva GS Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(3):66-9. PubMed ID: 2163174 [TBL] [Abstract][Full Text] [Related]
10. Syndrome identification case report 89: thickened subcutaneous tissue, coarse facies, macrocephaly, and hypotonia. Hillig U J Clin Dysmorphol; 1983; 1(1):9-12. PubMed ID: 6580387 [No Abstract] [Full Text] [Related]
12. Joubert syndrome co-existing with partial Xp trisomy: review of the literature. Güven GS; Fenerci EY; Deviren A; Ozkiliç A; Yüksel A; Hacihanefioğlu S Genet Couns; 2004; 15(3):321-8. PubMed ID: 15517825 [TBL] [Abstract][Full Text] [Related]
13. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage. Teebi AS; Shaltout AA Am J Med Genet; 1989 May; 33(1):58-60. PubMed ID: 2750786 [No Abstract] [Full Text] [Related]
14. Microcephaly, macrotia, unusual mimics and mental retardation syndrome: new syndrome or variant of De Lange type 2 syndrome. Verloes A; Lesenfants S; Philippet B; Iyawa A; Laloux F; Koulischer L Genet Couns; 1996; 7(4):277-82. PubMed ID: 8985731 [TBL] [Abstract][Full Text] [Related]
15. Anesthesia for a child with Kabuki Syndrome. Johnson G; Mayhew JF Paediatr Anaesth; 2007 Sep; 17(9):900-1. PubMed ID: 17683412 [No Abstract] [Full Text] [Related]
16. Trigonobrachycephaly, bulbous bifid nose, macrostomia, micrognathia, acral anomalies, and hypotonia in sibs. Teebi AS Am J Med Genet; 1991 Mar; 38(4):529-31. PubMed ID: 2063891 [No Abstract] [Full Text] [Related]
17. Uncombable hair syndrome, mental retardation, single palmar crease and arched palate in a patient with neurofibromatosis type I. Schena D; Germi L; Zamperetti MR; Darra F; Giacopuzzi S; Girolomoni G Pediatr Dermatol; 2007; 24(5):E73-5. PubMed ID: 17958786 [TBL] [Abstract][Full Text] [Related]
18. [Clinical considerations on a probable new case of the Coffin-Siris syndrome]. D'Elia R; Cassone L; Senatore A; Scianaro L; Loiodice G Minerva Pediatr; 1981 Oct; 33(20):1021-4. PubMed ID: 7311957 [No Abstract] [Full Text] [Related]
19. Ohdo-like blepharophimosis syndrome with distinctive facies, neonatal hypotonia, mental retardation and hypoplastic teeth. Clayton-Smith J; Krajewska-Walasek M; Fryer A; Donnai D Clin Dysmorphol; 1994 Apr; 3(2):115-20. PubMed ID: 8055130 [TBL] [Abstract][Full Text] [Related]