150 related articles for article (PubMed ID: 8305963)
1. Phenotypic correlations of ocular coloboma without known cause.
Leppig KA; Pagon RA
Clin Dysmorphol; 1993 Oct; 2(4):322-31. PubMed ID: 8305963
[TBL] [Abstract][Full Text] [Related]
2. Phenotypic variability of Cat-Eye syndrome.
Berends MJ; Tan-Sindhunata G; Leegte B; van Essen AJ
Genet Couns; 2001; 12(1):23-34. PubMed ID: 11332976
[TBL] [Abstract][Full Text] [Related]
3. Diagnostic precision in microphthalmos and coloboma of heterogeneous origin.
Warburg M
Birth Defects Orig Artic Ser; 1982; 18(6):31-50. PubMed ID: 7171763
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. Autosomal dominant typical coloboma associated with unilateral pseudoptosis, myopia and cataract.
Porges Y
Cent Afr J Med; 1995 Aug; 41(8):255-7. PubMed ID: 7585914
[TBL] [Abstract][Full Text] [Related]
8. Possible autosomal-recessive ocular coloboma.
Pagon RA; Kalina RE; Lechner DJ
Am J Med Genet; 1981; 9(3):189-93. PubMed ID: 7282780
[TBL] [Abstract][Full Text] [Related]
9. [Short stature, mental retardation, type I preaxial polydactyly with colobomatous abnormalities: a new syndrome].
Pfeiffer RA; Mayer U
Klin Monbl Augenheilkd; 1987 Dec; 191(6):473-7. PubMed ID: 3441111
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. Colobomatous malformations of the eye.
Maumenee IH; Mitchell TN
Trans Am Ophthalmol Soc; 1990; 88():123-32; discussion 133-5. PubMed ID: 2095017
[No Abstract] [Full Text] [Related]
12. Homonucleotide expansion and contraction mutations of PAX2 and inclusion of Chiari 1 malformation as part of renal-coloboma syndrome.
Schimmenti LA; Shim HH; Wirtschafter JD; Panzarino VA; Kashtan CE; Kirkpatrick SJ; Wargowski DS; France TD; Michel E; Dobyns WB
Hum Mutat; 1999; 14(5):369-76. PubMed ID: 10533062
[TBL] [Abstract][Full Text] [Related]
13. Further delineation of a syndrome of cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, coloboma, and hepatic fibrosis.
Verloes A; Lambotte C
Am J Med Genet; 1989 Feb; 32(2):227-32. PubMed ID: 2929661
[TBL] [Abstract][Full Text] [Related]
14. Ptosis, coloboma, hypertelorism and mental retardation.
Warburg M
Genet Couns; 1993; 4(1):69-70. PubMed ID: 8471225
[No Abstract] [Full Text] [Related]
15. Cytogenetics study in severely mentally retarded patients.
Yasseen AA; Al-Musawi TA
Saudi Med J; 2001 May; 22(5):444-9. PubMed ID: 11376389
[TBL] [Abstract][Full Text] [Related]
16. Microphthalmia, anophthalmia, and coloboma and associated ocular and systemic features: understanding the spectrum.
Skalicky SE; White AJ; Grigg JR; Martin F; Smith J; Jones M; Donaldson C; Smith JE; Flaherty M; Jamieson RV
JAMA Ophthalmol; 2013 Dec; 131(12):1517-24. PubMed ID: 24177921
[TBL] [Abstract][Full Text] [Related]
17. [An analysis of 193 cases of congenital intraocular colobomas].
Lu BX
Zhonghua Yan Ke Za Zhi; 1989 Nov; 25(6):357-9. PubMed ID: 2697542
[TBL] [Abstract][Full Text] [Related]
18. Congenital malformations of the eye. Report on 218 cases of grave reduction of vision caused by bilateral malformation of the ocular bulb.
Lindstedt E
Acta Ophthalmol (Copenh); 1968; 46(3):355-60. PubMed ID: 4974457
[No Abstract] [Full Text] [Related]
19. Mental retardation in amaurosis congenita of Leber.
Schuil J; Meire FM; Delleman JW
Neuropediatrics; 1998 Dec; 29(6):294-7. PubMed ID: 10029347
[TBL] [Abstract][Full Text] [Related]
20. Dominant inheritance of holoprosencephaly.
Cantú JM; Fragoso R; Garcia-Cruz D; Sánchez-Corona J
Birth Defects Orig Artic Ser; 1978; 14(6B):215-20. PubMed ID: 728563
[No Abstract] [Full Text] [Related]
[Next] [New Search]
