380 related articles for article (PubMed ID: 7810561)
1. 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]
2. 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]
3. 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]
4. KBG syndrome: review of the literature and findings of 5 affected patients.
Kumar H; Prabhu N; Cameron A
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Sep; 108(3):e72-9. PubMed ID: 19716495
[TBL] [Abstract][Full Text] [Related]
5. [Dento-maxillo-facial anomalies in the KBG syndrome].
Tollaro I; v Bassarelli ; Calzolari C; Franchini F; Giovannucci Uzielli ML; Vieri PL
Minerva Stomatol; 1984; 33(3):437-46. PubMed ID: 6589471
[No Abstract] [Full Text] [Related]
6. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
Filippi G
Am J Med Genet; 1985 Dec; 22(4):821-4. PubMed ID: 4073130
[TBL] [Abstract][Full Text] [Related]
7. Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis.
Toriello HV; Higgins JV
Am J Med Genet; 1995 Jan; 55(2):200-4. PubMed ID: 7717418
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Filippi syndrome: report of three additional cases.
Williams MS; Williams JL; Wargowski DS; Pauli RM; Pletcher BA
Am J Med Genet; 1999 Nov; 87(2):128-33. PubMed ID: 10533026
[TBL] [Abstract][Full Text] [Related]
10. Syndactyly type 1 with cataracts and mental retardation.
Pavone L; Fiumara A; Rizzo R; Parano E; Incorpora G
Clin Dysmorphol; 1993 Jul; 2(3):257-9. PubMed ID: 8287189
[TBL] [Abstract][Full Text] [Related]
11. [Cohen syndrome: report of two cases in female twins].
Arcas Martínez J; García Peñas JJ; Ramos Lizana J; Díaz González C; Pascual Castroviejo I
An Esp Pediatr; 1991 Jan; 34(1):83-5. PubMed ID: 2018266
[No Abstract] [Full Text] [Related]
12. Kabuki syndrome: a review.
Adam MP; Hudgins L
Clin Genet; 2005 Mar; 67(3):209-19. PubMed ID: 15691356
[TBL] [Abstract][Full Text] [Related]
13. Tapetoretinal degeneration and mental retardation associated with microspherophakia and mesodermal abnormalities: a new syndrome?
Sierpinski-Bart J; Neumann E; Tirosh E; Atias D
Metab Pediatr Ophthalmol; 1981; 5(3-4):225-31. PubMed ID: 6273671
[No Abstract] [Full Text] [Related]
14. A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto-nasal dysostosis, cleft lip/palate, limb hypoplasia, and postaxial poly-syndactyly: acro-fronto-facio-nasal dysostosis syndrome.
Richieri-Costa A; Colletto GM; Gollop TR; Masiero D
Am J Med Genet; 1985 Apr; 20(4):631-8. PubMed ID: 2986457
[TBL] [Abstract][Full Text] [Related]
15. KBG syndrome.
Brancati F; Sarkozy A; Dallapiccola B
Orphanet J Rare Dis; 2006 Dec; 1():50. PubMed ID: 17163996
[TBL] [Abstract][Full Text] [Related]
16. [Meyer-Schwickerath syndrome].
Huet F; Dascotte JC; Castier P
Bull Soc Ophtalmol Fr; 1988; 88(8-9):1017-9. PubMed ID: 2855044
[No Abstract] [Full Text] [Related]
17. The craniodigital syndrome of Scott: report of a second family.
Lorenz P; Hinkel GK; Hoffmann C; Rupprecht E
Am J Med Genet; 1990 Oct; 37(2):224-6. PubMed ID: 2174209
[TBL] [Abstract][Full Text] [Related]
18. New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement.
Borochowitz Z; Pavone L; Mazor G; Rizzo R; Dar H
Am J Med Genet; 1992 Jul; 43(4):678-85. PubMed ID: 1621757
[TBL] [Abstract][Full Text] [Related]
19. Fraser syndrome.
Chattopadhyay A; Kher AS; Udwadia AD; Sharma SV; Bharucha BA; Nicholson AD
J Postgrad Med; 1993; 39(4):228-30. PubMed ID: 7996504
[TBL] [Abstract][Full Text] [Related]
20. The Cohen syndrome in Israel.
Sack J; Friedman E
Isr J Med Sci; 1986 Nov; 22(11):766-70. PubMed ID: 2432032
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
