159 related articles for article (PubMed ID: 11992488)
1. Craniosynostosis, telecanthus, scalp hair abnormalities, and sensorineural deafness in two sibs.
Mégarbané A; Hersh JH; Chouery E; Fabre M
Am J Med Genet; 2002 May; 109(4):323-7. PubMed ID: 11992488
[TBL] [Abstract][Full Text] [Related]
2. Michels syndrome in a Brazilian girl born to consanguineous parents.
Guion-Almeida ML; Rodini ES
Am J Med Genet; 1995 Jul; 57(3):377-9. PubMed ID: 7677137
[TBL] [Abstract][Full Text] [Related]
3. Sensorineural hearing loss, enamel hypoplasia, and nail abnormalities in sibs.
Heimler A; Fox JE; Hershey JE; Crespi P
Am J Med Genet; 1991 May; 39(2):192-5. PubMed ID: 2063923
[TBL] [Abstract][Full Text] [Related]
4. Craniosynostosis and lid anomalies: report of a girl with Michels syndrome.
Cunniff C; Jones KL
Am J Med Genet; 1990 Sep; 37(1):28-30. PubMed ID: 2240039
[TBL] [Abstract][Full Text] [Related]
5. Pili torti and sensorineural hearing loss. A follow-up of Bjørnstad's original patients and a review of the literature.
Selvaag E
Eur J Dermatol; 2000 Mar; 10(2):91-7. PubMed ID: 10694305
[TBL] [Abstract][Full Text] [Related]
6. Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers.
Mégarbané A; Waked N; Chouery E; Moglabey YB; Saliba N; Mornet E; Serre JL; Slim R
Am J Med Genet; 2001 Jan; 98(3):244-9. PubMed ID: 11169562
[TBL] [Abstract][Full Text] [Related]
7. Stickler syndrome type I and Stapes ankylosis.
Baijens LW; De Leenheer EM; Weekamp HH; Cruysberg JR; Mortier GR; Cremers CW
Int J Pediatr Otorhinolaryngol; 2004 Dec; 68(12):1573-80. PubMed ID: 15533574
[TBL] [Abstract][Full Text] [Related]
8. Previously undescribed spondyloepiphyseal dysplasia associated with craniosynostosis, cataracts, cleft palate, and mental retardation: report of four sibs.
Nishimura G; Fukushima Y; Aihara T; Ohashi H; Nishimoto H; Nishimura J
Am J Med Genet; 1998 Apr; 77(1):1-7. PubMed ID: 9557884
[TBL] [Abstract][Full Text] [Related]
9. Neurologic anomalies of Perrault syndrome.
Gottschalk ME; Coker SB; Fox LA
Am J Med Genet; 1996 Nov; 65(4):274-6. PubMed ID: 8923934
[TBL] [Abstract][Full Text] [Related]
10. Additional case of Keipert syndrome and review of the literature.
Cappon SM; Khalifa MM
Med Sci Monit; 2000; 6(4):776-8. PubMed ID: 11208408
[TBL] [Abstract][Full Text] [Related]
11. Björnstad syndrome in a patient with mental retardation.
Van Buggenhout G; Trommelen J; Hamel B; Fryns JP
Genet Couns; 1998; 9(3):201-4. PubMed ID: 9777342
[TBL] [Abstract][Full Text] [Related]
12. Niikawa-Kuroki (Kabuki) syndrome with congenital sensorineural deafness: evidence for a wide spectrum of inner ear abnormalities.
Tekin M; Fitoz S; Arici S; Cetinkaya E; Incesulu A
Int J Pediatr Otorhinolaryngol; 2006 May; 70(5):885-9. PubMed ID: 16325926
[TBL] [Abstract][Full Text] [Related]
13. Shprintzen-Goldberg syndrome: a clinical analysis.
Greally MT; Carey JC; Milewicz DM; Hudgins L; Goldberg RB; Shprintzen RJ; Cousineau AJ; Smith WL; Judisch GF; Hanson JW
Am J Med Genet; 1998 Mar; 76(3):202-12. PubMed ID: 9508238
[TBL] [Abstract][Full Text] [Related]
14. Possible third case of Lin-Gettig syndrome.
Hedera P; Innis JW
Am J Med Genet; 2002 Jul; 110(4):380-3. PubMed ID: 12116213
[TBL] [Abstract][Full Text] [Related]
15. Further delineation of the Baller-Gerold syndrome.
Lin AE; McPherson E; Nwokoro NA; Clemens M; Losken HW; Mulvihill JJ
Am J Med Genet; 1993 Feb; 45(4):519-24. PubMed ID: 8465861
[TBL] [Abstract][Full Text] [Related]
16. Sensorineural deafness in two infants: a novel feature in the 22q distal duplication syndrome. Cardinal signs in trisomies 22 subtypes.
Barajas-Barajas LO; Valdez LL; Gonzalez JR; García-García C; Rivera H; Ramírez L
Genet Couns; 2004; 15(2):167-73. PubMed ID: 15287416
[TBL] [Abstract][Full Text] [Related]
17. Testicular cancer in a patient with Primrose syndrome.
Mathijssen IB; van Hasselt-van der Velde J; Hennekam RC
Eur J Med Genet; 2006; 49(2):127-33. PubMed ID: 16530709
[TBL] [Abstract][Full Text] [Related]
18. A variant of Fine-Lubinsky syndrome: a Japanese boy with profound deafness, cataracts, mental retardation, and brachycephaly without craniosynostosis.
Nakane T; Mizobe N; Hayashibe H; Nakazawa S
Clin Dysmorphol; 2002 Jul; 11(3):195-8. PubMed ID: 12072800
[TBL] [Abstract][Full Text] [Related]
19. Sensorineural hearing loss, small facial features, submucous cleft palate, and myoclonic seizures.
Preus M; Cooper AR; O'Leary E
J Clin Dysmorphol; 1984; 2(1):30-1. PubMed ID: 6587014
[No Abstract] [Full Text] [Related]
20. Vohwinkel syndrome with mental retardation.
Mercy P; Singh A; Ghorpade AK; Das MN; Upadhyay A; Keswani N
Indian J Dermatol Venereol Leprol; 2013; 79(5):725. PubMed ID: 23974601
[No Abstract] [Full Text] [Related]
[Next] [New Search]
