201 related articles for article (PubMed ID: 8471225)
1. Ptosis, coloboma, hypertelorism and mental retardation.
Warburg M
Genet Couns; 1993; 4(1):69-70. PubMed ID: 8471225
[No Abstract] [Full Text] [Related]
2. A new syndrome with ptosis, coloboma and mental retardation.
Le Marec B; Odent S; Urvoy M
Genet Couns; 1992; 3(2):119-20. PubMed ID: 1642810
[No Abstract] [Full Text] [Related]
3. Previously apparently undescribed syndrome: shallow orbits, ptosis, coloboma, trigonocephaly, gyral malformations, and mental and growth retardation.
Ramer JC; Lin AE; Dobyns WB; Winter R; Aymé S; Pallotta R; Ladda RL
Am J Med Genet; 1995 Jul; 57(3):403-9. PubMed ID: 7545868
[TBL] [Abstract][Full Text] [Related]
4. Iris coloboma, ptosis, hypertelorism, and mental retardation: Baraitser-Winter syndrome or Noonan syndrome?
Verloes A
J Med Genet; 1993 May; 30(5):425-6. PubMed ID: 8320709
[TBL] [Abstract][Full Text] [Related]
5. Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome possibly localised on chromosome 2.
Pallotta R
J Med Genet; 1991 May; 28(5):342-4. PubMed ID: 1865474
[TBL] [Abstract][Full Text] [Related]
6. Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome.
Baraitser M; Winter RM
J Med Genet; 1988 Jan; 25(1):41-3. PubMed ID: 3351890
[TBL] [Abstract][Full Text] [Related]
7. Hypertelorism, proptosis, ptosis, polysyndactyly, hypospadias and normal height in 3 sibs: a new syndrome?
Naguib KK
Am J Med Genet; 1988 Jan; 29(1):35-41. PubMed ID: 2830788
[No Abstract] [Full Text] [Related]
8. [Molecular diagnosis of CHARGE syndrom].
Pedersen AM; Skovby F
Ugeskr Laeger; 2007 Jan; 169(5):402-6. PubMed ID: 17280632
[TBL] [Abstract][Full Text] [Related]
9. [Extra mini-chromosome with symptoms of cat-eye syndrome].
Méhes K; Bajnóczky K; Schmidt P
Orv Hetil; 1985 Apr; 126(17):1037-9. PubMed ID: 3991187
[No Abstract] [Full Text] [Related]
10. Midline facial defects with ocular colobomata.
Temple IK; Brunner H; Jones B; Burn J; Baraitser M
Am J Med Genet; 1990 Sep; 37(1):23-7. PubMed ID: 1700608
[TBL] [Abstract][Full Text] [Related]
11. Malformative syndrome with trigonocephaly, shallow orbits, ptosis, growth and mental retardation. De novo autosomal reciprocal t(9;13)(Q32;Q22) in a male patient.
Fryns JP; Hendrickx G
Ann Genet; 1996; 39(1):51-3. PubMed ID: 9297446
[TBL] [Abstract][Full Text] [Related]
12. Wolf-Hirschhorn syndrome with posterior intraorbital coloboma cyst: an unusual case.
Tutunculer F; Acunas B; Hicdonmez T; Deviren A; Pelitli V
Brain Dev; 2004 Apr; 26(3):203-5. PubMed ID: 15030910
[TBL] [Abstract][Full Text] [Related]
13. [CHARGE association: 4 case reports].
Siala Gaigi S; Masmoudi A; Souissi MH; Chabchoub A; Chelli H; Khrouf N
Tunis Med; 1999 May; 77(5):297-302. PubMed ID: 10516817
[No Abstract] [Full Text] [Related]
14. X-linked syndrome of mental retardation, short stature, and hypertelorism: a new syndrome or a further example of the FG syndrome?
Bottani A
Am J Med Genet; 1994 May; 51(1):87-8. PubMed ID: 8030678
[No Abstract] [Full Text] [Related]
15. BBBG syndrome or Opitz syndrome: new family.
Verloes A; Le Merrer M; Briard ML
Am J Med Genet; 1989 Nov; 34(3):313-6. PubMed ID: 2688419
[TBL] [Abstract][Full Text] [Related]
16. The Dubowitz syndrome--one more case.
Chrzanowska KH; Krajewska-Walasek M
Klin Padiatr; 1987; 199(5):370-2. PubMed ID: 3316825
[TBL] [Abstract][Full Text] [Related]
17. Brief Clinical Report: coloboma hypospadias.
Halal F; Farsky K
Am J Med Genet; 1981; 8(1):53-8. PubMed ID: 7246606
[TBL] [Abstract][Full Text] [Related]
18. Mental retardation, microbrachycephaly, hypotelorism, palpebral ptosis, thin/long face, cleft lip, and lumbosacral/pelvic anomalies.
Richieri-Costa A; Guion-Almeida ML; Ramos AL
Am J Med Genet; 1992 Jun; 43(3):565-8. PubMed ID: 1605250
[TBL] [Abstract][Full Text] [Related]
19. Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?
Donnai D; Barrow M
Am J Med Genet; 1993 Oct; 47(5):679-82. PubMed ID: 8266995
[TBL] [Abstract][Full Text] [Related]
20. The phenotypic spectrum of baraitser-winter syndrome: a new case and review of literature.
Ganesh A; Al-Kindi A; Jain R; Raeburn S
J AAPOS; 2005 Dec; 9(6):604-6. PubMed ID: 16414535
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]