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Date: 1997
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/187091
Description: Reply to Eli Hatchwell's Letter to the Editor, "Shprintzen-Goldberg syndrome results from mutations in fibrillin-1, not monosomy 22q11". (http//dx.doi.org/10.1016/S0022-3476(97)70144-6)
Date: 1995
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/186703
Description: Interstitial deletions in chromosome 22 and features associated with CATCH-22 syndrome have been reported in patients with conotruncal congenital head anomalies. Absent pulmonary valve syndrome is cha ... More
Reviewed: Reviewed
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