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8. 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]
9. [Kabuki syndrome in the differential diagnosis of neonatal hypotonia]. Aguilera Albesa S; Botella Astorqui MP; Ocio Ocio I An Pediatr (Barc); 2009 Jan; 70(1):91-3. PubMed ID: 19174128 [No Abstract] [Full Text] [Related]
10. Syndrome identification case report 100: unusual facies, cleft palate, short stature, and mental retardation. Feingold M; Trainer J J Clin Dysmorphol; 1983; 1(2):22-3. PubMed ID: 6580391 [No Abstract] [Full Text] [Related]
11. New case of the Carey-Fineman-Ziter syndrome. Baraitser M; Reardon W Am J Med Genet; 1994 Nov; 53(2):163-4. PubMed ID: 7856641 [TBL] [Abstract][Full Text] [Related]
12. Megalocornea-mental retardation syndrome: an additional case. Antiñolo G; Rufo M; Borrego S; Morales C Am J Med Genet; 1994 Aug; 52(2):196-7. PubMed ID: 7802008 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. A familial syndrome with hypotonia, mental retardation and dysmorphic features resembling Cohen syndrome. Mejía-Baltodano G; Bobadilla L; Solís A; Mendoza R; Díaz-Gallardo MY; Barros-Núñez P Genet Couns; 1997; 8(4):311-6. PubMed ID: 9457500 [TBL] [Abstract][Full Text] [Related]
15. Adrenal insufficiency, myopathic hypotonia, severe psychomotor retardation, failure to thrive, constipation and bladder ectasia in 2 brothers: adrenomyodystrophy. von Petrykowski W; Beckmann R; Böhm N; Ketelsen UP; Ropers HH; Sauer M Helv Paediatr Acta; 1982 Sep; 37(4):387-400. PubMed ID: 7153060 [TBL] [Abstract][Full Text] [Related]
16. [Syndrome Mulibrey Nanism. A case report and autopsy findings in a 8-month-old girl (author's transl)]. Finni K; Herva R Klin Padiatr; 1981 Jul; 193(4):328-30. PubMed ID: 7265804 [No Abstract] [Full Text] [Related]
17. Varadi-Papp syndrome: report of a case. Mauceri L; Greco F; Baieli S; Sorge G Clin Dysmorphol; 2000 Oct; 9(4):289-90. PubMed ID: 11045588 [TBL] [Abstract][Full Text] [Related]
18. Fusion of vertebrae, diaphragmatic hernia and unusual facies in a girl: a possible further case of Mathieu syndrome. Zelante L; Ruscitto MM Clin Dysmorphol; 2003 Jul; 12(3):207-8. PubMed ID: 14564164 [TBL] [Abstract][Full Text] [Related]
19. [Coffin-Siris syndrome. Critical study of the literature apropos of a case]. Foasso MF; Hermier M; Descos B; Collet JP; Perron F Pediatrie; 1983 Mar; 38(2):111-7. PubMed ID: 6622139 [TBL] [Abstract][Full Text] [Related]
20. [Werdnig-Hoffmann disease in 2 siblings]. Zajadacz B Pol Tyg Lek; 1979 May; 34(21):837-8. PubMed ID: 471820 [No Abstract] [Full Text] [Related] [Next] [New Search]