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22. [Supravalvular aortic stenosis, mental retardation, and peculiar facies]. Beaudoing A; Hadjian AJ; Bost M; Jourdain JA Pediatrie; 1971 Jun; 26(4):436-7. PubMed ID: 5568953 [No Abstract] [Full Text] [Related]
23. A syndrome manifested by brittle hair with morphologic and biochemical abnormalities, developmental delay and normal stature. Arbisser AI; Scott CI; Howell RR; Ong PS; Cox HL Birth Defects Orig Artic Ser; 1976; 12(5):219-28. PubMed ID: 953226 [TBL] [Abstract][Full Text] [Related]
24. [The Freeman-Sheldon syndrome with mental retardation]. Cirillo Silengo M; Davi GF; Bianco R; De Marco A; Costa M; Franceschini P; Bonenti G Minerva Pediatr; 1982 Mar; 34(6):277-80. PubMed ID: 6808331 [No Abstract] [Full Text] [Related]
25. Cohen syndrome. Alavi S; Kher A; Kumar A; Muranjan M; Bharucha B Indian Pediatr; 1993 May; 30(5):678-81. PubMed ID: 8282400 [No Abstract] [Full Text] [Related]
26. Characteristic facial dysmorphism, arachnodactyly and mental handicap in two unrelated girls: a distinct MCA/MR syndrome? de Die-Smulders C; Vles H; Fryns JP Genet Couns; 1993; 4(2):165-7. PubMed ID: 8357568 [TBL] [Abstract][Full Text] [Related]
27. Unusual features in eyelid myoclonia with absences: a patient with mild mental retardation and background slowing on electroencephalography. Sevgi Demirci EB; Saygi S Epilepsy Behav; 2006 Mar; 8(2):442-5. PubMed ID: 16446119 [TBL] [Abstract][Full Text] [Related]
35. New MCA/MR syndrome with generalized hypotonia, congenital hydronephrosis, and characteristic face. Okamoto N; Matsumoto F; Shimada K; Satomura K Am J Med Genet; 1997 Jan; 68(3):347-9. PubMed ID: 9024570 [TBL] [Abstract][Full Text] [Related]
36. Mental retardation, abnormal hair and mild aminoaciduria, all of unknown aetiology, in siblings. Mann TP Proc R Soc Med; 1969 Apr; 62(4):328. PubMed ID: 5811937 [No Abstract] [Full Text] [Related]
37. Hypotonic syndrome accompanied by paroxysmal paralyses and skew deviation. Havlová M; Otradovec J; Dittrich J Acta Univ Carol Med Monogr; 1976; (75):54-5. PubMed ID: 1088730 [No Abstract] [Full Text] [Related]
38. [Indication and value of trichoglyphic examinations]. Katalin K; Magdolna M; Péter L Orv Hetil; 1977 Mar; 118(12):675-7. PubMed ID: 846708 [No Abstract] [Full Text] [Related]
39. [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]
40. Facio-cutaneous-skeletal syndrome is the Costello syndrome. Martin RA; Jones KL Am J Med Genet; 1993 Aug; 47(2):169, 73. PubMed ID: 8213899 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]