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<article  article-type="case-report"        dtd-version="1.4">
            <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>
                                                                                                                        <trans-title-group xml:lang="en">
                                    <trans-title>A New Chromosome Breakage Syndrome</trans-title>
                                </trans-title-group>
                                                                                                                                                                                                <article-title>Yeni Bir Kromozom Kırığı Sendromu</article-title>
                                                                                                    </title-group>
            
                                                    <contrib-group content-type="authors">
                                                                        <contrib contrib-type="author">
                                                                <name>
                                    <surname>Şaylı</surname>
                                    <given-names>B. Sıtkı</given-names>
                                </name>
                                                                    <aff>ANKARA ÜNİVERSİTESİ, TIP FAKÜLTESİ, DAHİLİ TIP BİLİMLERİ BÖLÜMÜ, TIBBİ GENETİK ANABİLİM DALI</aff>
                                                            </contrib>
                                                                                </contrib-group>
                        
                                        <pub-date pub-type="pub" iso-8601-date="19721231">
                    <day>12</day>
                    <month>31</month>
                    <year>1972</year>
                </pub-date>
                                        <volume>25</volume>
                                        <issue>6</issue>
                                        <fpage>1396</fpage>
                                        <lpage>1401</lpage>
                        
                        <history>
                                    <date date-type="received" iso-8601-date="19721101">
                        <day>11</day>
                        <month>01</month>
                        <year>1972</year>
                    </date>
                                                    <date date-type="accepted" iso-8601-date="19721230">
                        <day>12</day>
                        <month>30</month>
                        <year>1972</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>
            
                                                                                                <trans-abstract xml:lang="en">
                            <p>We present in this paper a family with classical Huntingtons chorea in two members of which, proband and her asymptomatic son, choromozom analyses of peripheral blood cells reveals a high percentages of choromatide breaks (9,6 - 3,3 percent, respectively) and a high proportion of hypodiploid plates. Both findinges have be considered of some significance.</p></trans-abstract>
                                                                                                                                    <abstract><p>Klasik Huntington Koreli hanım ve normal görünümlü oğlunun periferik kanlarından hazırlanan metafaz plâklarının incelenmesinde normalde rastladığımızın üstünde (annede 9.6, oğulda % 4,3) kromatid kırıklarına ve yüksek oranda hypoploid plâklara rastlanmıştır. Bu bulgular bir kırık sendromu karşısında kaldığımız şeklinde yorumlanmıştır.</p></abstract>
                                                            
            
                                                                                        <kwd-group>
                                                    <kwd>Genetik</kwd>
                                                    <kwd>  Kromozom</kwd>
                                                    <kwd>  Kırık</kwd>
                                            </kwd-group>
                            
                                                <kwd-group xml:lang="en">
                                                    <kwd>Genetic</kwd>
                                                    <kwd>  Chromosome</kwd>
                                                    <kwd>  breakage</kwd>
                                            </kwd-group>
                                                                                                                                    <funding-group specific-use="FundRef">
                    <award-group>
                                                    <funding-source>
                                <named-content content-type="funder_name">Ankara Üniversitesi Tıp Fakültesi Genetik Kürsüsü ve Psikiyatri Kliniği</named-content>
                            </funding-source>
                                                                    </award-group>
                </funding-group>
                                </article-meta>
    </front>
    <back>
                            <ref-list>
                                    <ref id="ref1">
                        <label>1</label>
                        <mixed-citation publication-type="journal">1- BARBEAU,. A. Parant ascent in the juvenile form of Huntington&#039;s chorea LANCET 2: 937, (1970).</mixed-citation>
                    </ref>
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                                    <ref id="ref6">
                        <label>6</label>
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                    </ref>
                                    <ref id="ref7">
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                    </ref>
                                    <ref id="ref9">
                        <label>9</label>
                        <mixed-citation publication-type="journal">9- KOBİERSKİ, W. Cytogenetic analyse in elderly women. POL. TYGİLEK 25/35, 1313, (1970).</mixed-citation>
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                                    <ref id="ref10">
                        <label>10</label>
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                            </ref-list>
                    </back>
    </article>
