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3. Macrocephaly with hamartomas: Bannayan-Zonana syndrome. Miles JH; Zonana J; Mcfarlane J; Aleck KA; Bawle E Am J Med Genet; 1984 Oct; 19(2):225-34. PubMed ID: 6507473 [TBL] [Abstract][Full Text] [Related]
4. Bannayan-Riley-Ruvalcaba syndrome. Gorlin RJ; Cohen MM; Condon LM; Burke BA Am J Med Genet; 1992 Oct; 44(3):307-14. PubMed ID: 1336932 [TBL] [Abstract][Full Text] [Related]
5. Calcifying epithelioma of Malherbe. Association with myotonic muscular dystrophy. Harper PS Arch Dermatol; 1972 Jul; 106(1):41-4. PubMed ID: 5039107 [No Abstract] [Full Text] [Related]
6. Macrocephaly, multiple lipomas, and hemangiomata (Bannayan-Zonana syndrome): genetic heterogeneity or autosomal dominant locus with at least two different allelic forms? Moretti-Ferreira D; Koiffmann CP; Souza DH; Diament AJ; Wajntal A Am J Med Genet; 1989 Dec; 34(4):548-51. PubMed ID: 2624267 [TBL] [Abstract][Full Text] [Related]
7. Excessive high voltage fast activity in familial mental retardation, hyperkinesis and macrocephaly. Bogart KC; Froozan H Electroencephalogr Clin Neurophysiol; 1970 Apr; 28(4):419-20. PubMed ID: 4191203 [No Abstract] [Full Text] [Related]
8. The Bannayan syndrome: an autosomal dominant disorder consisting of macrocephaly, lipomas, hemangiomas, and risk for intracranial tumors. Higginbottom MC; Schultz P Pediatrics; 1982 May; 69(5):632-4. PubMed ID: 7079022 [TBL] [Abstract][Full Text] [Related]
9. Costello syndrome: report of an 8-month-old marasmic boy. Popa M; Ioan DM; Fryns JP Genet Couns; 1996; 7(1):27-30. PubMed ID: 8652085 [TBL] [Abstract][Full Text] [Related]
10. Schizophrenia and mental retardation associated in a pedigree with retinitis pigmentosa and sensorineural deafness. Sharp CW; Muir WJ; Blackwood DH; Walker M; Gosden C; St Clair DM Am J Med Genet; 1994 Dec; 54(4):354-60. PubMed ID: 7726208 [TBL] [Abstract][Full Text] [Related]
11. Macrocephaly with multiple lipomas and hemangiomas. Zonana J; Rimoin DL; Davis DC J Pediatr; 1976 Oct; 89(4):600-3. PubMed ID: 957004 [No Abstract] [Full Text] [Related]
12. A distinctive syndrome of brachycephaly, deafness, cataracts and mental retardation. Suthers GK; Earley AE; Huson SM Clin Dysmorphol; 1993 Oct; 2(4):342-5. PubMed ID: 7508318 [TBL] [Abstract][Full Text] [Related]
13. Alopecia-mental retardation syndrome: clinical and molecular characterization of four patients. Tzschach A; Bozorgmehr B; Hadavi V; Kahrizi K; Garshasbi M; Motazacker MM; Ropers HH; Kuss AW; Najmabadi H Br J Dermatol; 2008 Sep; 159(3):748-51. PubMed ID: 18616779 [No Abstract] [Full Text] [Related]
14. Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndrome. Reardon W; Gibbons RJ; Winter RM; Baraitser M Am J Med Genet; 1995 Jan; 55(3):285-7. PubMed ID: 7726224 [TBL] [Abstract][Full Text] [Related]
15. New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early death. Gustavson KH; Annerén G; Malmgren H; Dahl N; Ljunggren CG; Bäckman H Am J Med Genet; 1993 Mar; 45(5):654-8. PubMed ID: 8456840 [TBL] [Abstract][Full Text] [Related]
16. [Orthodontic aspects in a case of orofaciodigital syndrome]. Dambrain R Acta Stomatol Belg; 1967; 64(2):233-47. PubMed ID: 5233864 [No Abstract] [Full Text] [Related]
17. Escalante syndrome and the marker X chromosome. Vianna-Morgante AM; Armando I; Frota-Pessoa O Am J Med Genet; 1982 Jun; 12(2):237-40. PubMed ID: 7201744 [No Abstract] [Full Text] [Related]
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19. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation. Brooks SS; Wisniewski K; Brown WT Am J Med Genet; 1994 Jul; 51(4):586-90. PubMed ID: 7943044 [TBL] [Abstract][Full Text] [Related]