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2. Coffin-Lowry syndrome and premature tooth loss: a case report. Day P; Cole B; Welbury R ASDC J Dent Child; 2000; 67(2):148-50. PubMed ID: 10826053 [TBL] [Abstract][Full Text] [Related]
3. Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria. Zollino M; Battaglia A; D'Avanzo MG; Della Bruna MM; Marini R; Scarano G; Cappa M; Neri G Am J Med Genet; 1994 Sep; 52(3):302-7. PubMed ID: 7810561 [TBL] [Abstract][Full Text] [Related]
4. The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies. Herrmann J; Pallister PD; Tiddy W; Opitz JM Birth Defects Orig Artic Ser; 1975; 11(5):7-18. PubMed ID: 1218237 [No Abstract] [Full Text] [Related]
5. A new X-linked multiple congenital anomalies/mental retardation syndrome. Golabi M; Ito M; Hall BD Am J Med Genet; 1984 Jan; 17(1):367-74. PubMed ID: 6711604 [TBL] [Abstract][Full Text] [Related]
6. Lapsus--caveat emptor: Coffin-Lowry syndrome vs Coffin-Siris syndrome--an example of confusion compounded. Gorlin RJ Am J Med Genet; 1981; 10(1):103-4. PubMed ID: 7294058 [No Abstract] [Full Text] [Related]
7. Coffin-Lowry syndrome: clinical aspects at different ages and symptoms in female carriers. Plomp AS; De Die-Smulders CE; Meinecke P; Ypma-Verhulst JM; Lissone DA; Fryns JP Genet Couns; 1995; 6(3):259-68. PubMed ID: 8588856 [TBL] [Abstract][Full Text] [Related]
8. The KBG syndrome: an additional sporadic case. Mathieu M; Helou M; Morin G; Dolhem P; Devauchelle B; Piussan C Genet Couns; 2000; 11(1):33-5. PubMed ID: 10756425 [TBL] [Abstract][Full Text] [Related]
9. [Coffin-Lowry syndrome. Description of 2 cases associated with cardiovascular anomalies]. Della Cella G; Stagnaro MG; Beluschi C; Forni GL Pediatr Med Chir; 1987; 9(2):229-32. PubMed ID: 3658807 [TBL] [Abstract][Full Text] [Related]
11. Coffin-Lowry syndrome in sibs. Mattei JF; Laframboise R; Rouault F; Giraud F Am J Med Genet; 1981; 8(3):315-9. PubMed ID: 7234901 [No Abstract] [Full Text] [Related]
12. W syndrome: report of three cases and review. Goizet C; Bonneau D; Lacombe D Am J Med Genet; 1999 Dec; 87(5):446-9. PubMed ID: 10594887 [TBL] [Abstract][Full Text] [Related]
13. Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22. Bird H; Collins AL; Oley C; Lindsay S Am J Med Genet; 1995 Dec; 59(4):512-6. PubMed ID: 8585574 [TBL] [Abstract][Full Text] [Related]
14. Japanese kindred with FG syndrome. Kato R; Niikawa N; Nagai T; Fukushima Y Am J Med Genet; 1994 Aug; 52(2):242-3. PubMed ID: 7802020 [No Abstract] [Full Text] [Related]
17. Mental retardation, deafness, skeletal abnormalities, and coarse face with full lips: confirmation of the Fountain syndrome. Fryns JP; Dereymaeker A; Hoefnagels M; Van den Berghe H Am J Med Genet; 1987 Mar; 26(3):551-5. PubMed ID: 3565469 [TBL] [Abstract][Full Text] [Related]
19. [Coffin-Lowry syndrome. Description of 2 cases]. Barajas LO; Rivera H; Fragoso R; Nazara Z; CantĂș JM Bol Med Hosp Infant Mex; 1986 Jun; 43(6):378-81. PubMed ID: 3730116 [No Abstract] [Full Text] [Related]
20. A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndrome. Bottani A; Schinzel A Clin Dysmorphol; 1993 Jul; 2(3):225-31. PubMed ID: 8287184 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]