Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 237

Related Citations for PubMed (Select 8574420)

1.

Absent iris stroma, narrow body build and small facial bones: a new association or variant of SHORT syndrome?

Bankier A, Keith CG, Temple IK.

Clin Dysmorphol. 1995 Oct;4(4):304-12.

PMID:
8574420
2.

Rieger anomaly and congenital glaucoma in the SHORT syndrome.

Brodsky MC, Whiteside-Michel J, Merin LM.

Arch Ophthalmol. 1996 Sep;114(9):1146-7. No abstract available.

PMID:
8790109
3.

Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct.

Walter MA, Mirzayans F, Mears AJ, Hickey K, Pearce WG.

Ophthalmology. 1996 Nov;103(11):1907-15.

PMID:
8942889
5.

SHORT syndrome: a new case with probable autosomal dominant inheritance.

Sorge G, Ruggieri M, Polizzi A, Scuderi A, Di Pietro M.

Am J Med Genet. 1996 Jan 11;61(2):178-81.

PMID:
8669449
6.

A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene.

Honkanen RA, Nishimura DY, Swiderski RE, Bennett SR, Hong S, Kwon YH, Stone EM, Sheffield VC, Alward WL.

Am J Ophthalmol. 2003 Mar;135(3):368-75.

PMID:
12614756
7.

SHORT syndrome.

Koenig R, Brendel L, Fuchs S.

Clin Dysmorphol. 2003 Jan;12(1):45-9. Review.

PMID:
12514365
8.

A new syndrome with distinct facial and auricular malformations and dominant inheritance.

Simosa V, Penchaszadeh VB, Bustos T.

Am J Med Genet. 1989 Feb;32(2):184-6.

PMID:
2929657
9.

Axenfeld-Rieger syndrome. A spectrum of developmental disorders.

Shields MB, Buckley E, Klintworth GK, Thresher R.

Surv Ophthalmol. 1985 May-Jun;29(6):387-409. Review.

PMID:
3892740
10.

Rieger syndrome.

Deng J, Wang N.

Yan Ke Xue Bao. 1998 Mar;14(1):52-6.

PMID:
12580078
11.

Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.

Yüksel A, Seven M, Deviren A, Söylemez MA, Hacihanefioğlu S, Ulutin T, Cenani A.

Genet Couns. 1999;10(3):265-9.

PMID:
10546098
12.

Cardiovascular anomaly in Rieger Syndrome: heterogeneity or contiguity?

Mammi I, De Giorgio P, Clementi M, Tenconi R.

Acta Ophthalmol Scand. 1998 Aug;76(4):509-12. Review.

PMID:
9716345
13.

Smith-Fineman-Myers syndrome: report of a third case.

Stephenson LD, Johnson JP.

Am J Med Genet. 1985 Oct;22(2):301-4.

PMID:
4050861
14.

Iris transillumination defects associated with pallister-killian syndrome.

Ticho BH.

J Pediatr Ophthalmol Strabismus. 2010 Jan-Feb;47(1):58-9. doi: 10.3928/01913913-20100106-14. Epub 2010 Jan 21.

PMID:
20128558
15.

A distinct dysmorphic syndrome with congenital glaucoma and probable autosomal recessive inheritance.

García-Cruz D, Mendoza R, Villar V, Sanchez-Corona J, García-Cruz MO, Rojas Q, Chavez-Anaya F, Nazara Z, Barrios MT, Cantu JM.

Ophthalmic Paediatr Genet. 1990 Mar;11(1):35-40.

PMID:
2348980
16.

Rieger's syndrome: a case report.

Prabhu NT, John R, Munshi AK.

Quintessence Int. 1997 Nov;28(11):749-52. Review.

PMID:
9573866
17.

Provisionally unique autosomal recessive chondrodysplasia punctata syndrome.

Toriello HV, Higgins JV, Miller T.

Am J Med Genet. 1993 Oct 1;47(5):797-9.

PMID:
8267015
18.

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.

PMID:
1700608
19.

The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype.

Tekin M, Kavaz A, Berberoğlu M, Fitoz S, Ekim M, Ocal G, Akar N.

Am J Med Genet A. 2004 Oct 15;130A(3):284-7. Review.

PMID:
15378538
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk