Prenatal diagnosis for primary congenital glaucoma (bupthalmous) [8]

Prenatal Diagnosis

Volumn 26, Issue 9, 2006, Pages 877-

  Strom, Charles M ^a   Strom, Sam ^b   Redman, Joy ^a   Sun, Weimin ^a  

^a QUEST DIAGNOSTICS NICHOLS INSTITUTE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; CASE REPORT; CLINICAL FEATURE; DNA SEQUENCE; FEMALE; GLAUCOMA; HUMAN; LETTER; PRENATAL DIAGNOSIS; PRESCHOOL CHILD; PRIMARY CONGENITAL GLAUCOMA; PRIORITY JOURNAL;

ARYL HYDROCARBON HYDROXYLASES; CHILD, PRESCHOOL; CHORIONIC VILLI SAMPLING; DISEASES IN TWINS; FEMALE; HUMANS; HYDROPHTHALMOS; MUTATION; PRENATAL DIAGNOSIS;

EID: 33749497300     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.1538     Document Type: Letter

References (2)

1. Ho CL, Walton DS. 2004. Primary congenital glaucoma, 2004 update. J Pediatr Ophthalmol Strabismus 41: 271-288.
2. Stoilov I, Akarsu N, Alozie I, et al. 1998. Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome p4501Bl. Am J Hum Genet 62: 573-584.