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            <front>

                <journal-meta>
                                    <journal-id></journal-id>
            <journal-title-group>
                                                                                    <journal-title>Ankara Üniversitesi Tıp Fakültesi Mecmuası</journal-title>
            </journal-title-group>
                            <issn pub-type="ppub">0365-8104</issn>
                                        <issn pub-type="epub">1307-5608</issn>
                                                                                            <publisher>
                    <publisher-name>Ankara University</publisher-name>
                </publisher>
                    </journal-meta>
                <article-meta>
                                        <article-id/>
                                                                <article-categories>
                                            <subj-group  xml:lang="en">
                                                            <subject>Medical Genetics (Excl. Cancer Genetics)</subject>
                                                    </subj-group>
                                            <subj-group  xml:lang="tr">
                                                            <subject>Tıbbi Genetik (Kanser Genetiği hariç)</subject>
                                                    </subj-group>
                                    </article-categories>
                                                                                                                                                        <title-group>
                                                                                                                                                            <article-title>Homocystinuria : Report Of Three Cases</article-title>
                                                                                                    </title-group>
            
                                                    <contrib-group content-type="authors">
                                                                        <contrib contrib-type="author">
                                                                <name>
                                    <surname>Türmen</surname>
                                    <given-names>Tomris</given-names>
                                </name>
                                                                    <aff>ANKARA UNIVERSITY, ANKARA FACULTY OF MEDICINE</aff>
                                                            </contrib>
                                                                                </contrib-group>
                        
                                        <pub-date pub-type="pub" iso-8601-date="19771231">
                    <day>12</day>
                    <month>31</month>
                    <year>1977</year>
                </pub-date>
                                        <volume>30</volume>
                                        <issue>4</issue>
                                        <fpage>837</fpage>
                                        <lpage>843</lpage>
                        
                        <history>
                                    <date date-type="received" iso-8601-date="19771001">
                        <day>10</day>
                        <month>01</month>
                        <year>1977</year>
                    </date>
                                                    <date date-type="accepted" iso-8601-date="19771230">
                        <day>12</day>
                        <month>30</month>
                        <year>1977</year>
                    </date>
                            </history>
                                        <permissions>
                    <copyright-statement>Copyright © 1947, Ankara Üniversitesi Tıp Fakültesi Mecmuası</copyright-statement>
                    <copyright-year>1947</copyright-year>
                    <copyright-holder>Ankara Üniversitesi Tıp Fakültesi Mecmuası</copyright-holder>
                </permissions>
            
                                                                                                                        <abstract><p>Three cases of homocystinuria which is one of the most common inborn &amp;amp;rrrors of metabolism are presented and methionin metabolism and therapeutic approaches in homocystinuria are reviewed.</p></abstract>
                                                            
            
                                                                                        <kwd-group>
                                                    <kwd>genetics</kwd>
                                                    <kwd>  Homocystinuria</kwd>
                                                    <kwd>  methionin</kwd>
                                            </kwd-group>
                            
                                                                                                                                                    </article-meta>
    </front>
    <back>
                            <ref-list>
                                    <ref id="ref1">
                        <label>1</label>
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                    </ref>
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                        <label>2</label>
                        <mixed-citation publication-type="journal">2.	Carson, N.AJ., Cusworth, D.C., Dent, C.E. et. al. : Homocystinuria : a new inborn error of metabolism associated with mental deficiency. Arch. Dis. Child. 38 : 425, 1963.</mixed-citation>
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                        <mixed-citation publication-type="journal">6.	Morrov, G. and Barness, L.A. : Combined vitamin responsiveness in homocystinurla, J. Pediatr. 81 : 946, 1972.</mixed-citation>
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                        <mixed-citation publication-type="journal">9.	McDonald, L., Bray, C., Field, C., Love, F. and Davies, B. : Homocystinuria, thrombosis and the blood platelets. Lancet | : 745, 1964.</mixed-citation>
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                        <label>12</label>
                        <mixed-citation publication-type="journal">12.	Golstein, J.L,, Campell, B.K. and Gartler, S.M. : Homocystinuria : Heterozygote detection using phytohemagglutinin stimulated Iymhocytes. J. Clin. İnvest. 52 ; 218, 1973.</mixed-citation>
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                        <mixed-citation publication-type="journal">14.	Homocystinuria : Investigation of cystationine synthase in cultured fetal cells and prenatal determination of genetic status. J. Pediatr. 85 : 677, 1974,</mixed-citation>
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                        <mixed-citation publication-type="journal">16.	Longlu, R.C., Fleisher L.D., Tallon H.H, Gaull, G.E. : Cystationine B-synthase defiency : a gualitative abnormality of the deficient enzyme modified by Vit. B; therapy. Ped. Res. 11 : 110, 1977,</mixed-citation>
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                            </ref-list>
                    </back>
    </article>
