Please use this identifier to cite or link to this item: http://hdl.handle.net/1959.14/187091
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- Title
- Reply
- Related
- Journal of pediatrics, Vol. 131, Issue 1, Part 1, (1997), p.165-165
- DOI
- 10.1016/S0022-3476(97)70145-8
- Publisher
- Mosby, Inc
- Date
- 1997
- Author/Creator
- Johnson, Mark C
- Author/Creator
- Watson, Michael S
- Author/Creator
- Dowton, S. Bruce
- Author/Creator
- Strauss, Arnold W
- 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)
- Description
- 1 page(s)
- Resource Type
- journal article
- Organisation
- Macquarie University. Office of the Vice-Chancellor
- Identifier
- http://hdl.handle.net/1959.14/187091
- Identifier
- ISSN:0022-3476
- Identifier
- mq_res-ext-2-s2.0-0030722119
- Language
- eng
