{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,13]],"date-time":"2026-04-13T13:47:00Z","timestamp":1776088020469,"version":"3.50.1"},"reference-count":25,"publisher":"Wiley","issue":"8","license":[{"start":{"date-parts":[[2020,5,12]],"date-time":"2020-05-12T00:00:00Z","timestamp":1589241600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"},{"start":{"date-parts":[[2020,5,12]],"date-time":"2020-05-12T00:00:00Z","timestamp":1589241600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/501100004881","name":"Instituto Mexicano del Seguro Social","doi-asserted-by":"publisher","award":["FIS\/IMSS\/PROT\/G18\/1817"],"award-info":[{"award-number":["FIS\/IMSS\/PROT\/G18\/1817"]}],"id":[{"id":"10.13039\/501100004881","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Laboratory Analysis"],"published-print":{"date-parts":[[2020,8]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Non\u2010acrocentric satellited chromosomes mostly result from familial balanced insertions or translocations with p12 or p13 of any acrocentric. Although all non\u2010acrocentrics have been involved, only 12 instances of chromosome 6 involvement are known.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Case presentation<\/jats:title>\n                    <jats:p>\n                      A female infant exhibited clinical features typical of 6qter deletions and also generalized hypertrichosis and synophrys, traits seldom reported in patients with similar imbalances or haploinsufficiency of\n                      <jats:italic>ARID1B<\/jats:italic>\n                      located in 6q25.3. She had a paternal derivative satellited 6q of a t(6;22)(q25.3;p12)pat entailing a 6q terminal deletion, karyotype 46,XX,der(6)t(6;22)(q25.3;p12)pat [16].ish del 6q subtel\u2013.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>Male and female carriers of reciprocal translocations or insertions between chromosome 6 and the short arm of any acrocentric have few unbalanced offspring mostly by adjacent\u20101 segregation. In addition, spontaneous abortions or male infertility was present in 7\/13 instances of satellited chromosome 6.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/jcla.23355","type":"journal-article","created":{"date-parts":[[2020,5,13]],"date-time":"2020-05-13T01:33:05Z","timestamp":1589333585000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short\u2010lived infant"],"prefix":"10.1002","volume":"34","author":[{"given":"Mar\u00eda Guadalupe","family":"Dom\u00ednguez","sequence":"first","affiliation":[{"name":"Divisi\u00f3n de Gen\u00e9tica CIBO Instituto Mexicano del Seguro Social Guadalajara M\u00e9xico"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Horacio","family":"Rivera","sequence":"additional","affiliation":[{"name":"Divisi\u00f3n de Gen\u00e9tica CIBO Instituto Mexicano del Seguro Social Guadalajara M\u00e9xico"},{"name":"Doctorado en Gen\u00e9tica Humana CUCS Universidad de Guadalajara Guadalajara M\u00e9xico"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rosa Mar\u00eda","family":"D\u00e1valos\u2010Pulido","sequence":"additional","affiliation":[{"name":"Divisi\u00f3n de Gen\u00e9tica CIBO Instituto Mexicano del Seguro Social Guadalajara M\u00e9xico"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ingrid Patricia","family":"D\u00e1valos\u2010Rodr\u00edguez","sequence":"additional","affiliation":[{"name":"Divisi\u00f3n de Gen\u00e9tica CIBO Instituto Mexicano del Seguro Social Guadalajara M\u00e9xico"},{"name":"Doctorado en Gen\u00e9tica Humana CUCS Universidad de Guadalajara Guadalajara M\u00e9xico"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2020,5,12]]},"reference":[{"key":"e_1_2_9_2_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00279007"},{"key":"e_1_2_9_3_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.34259"},{"key":"e_1_2_9_4_1","doi-asserted-by":"publisher","DOI":"10.1034\/j.1399-0004.2000.580411.x"},{"key":"e_1_2_9_5_1","doi-asserted-by":"publisher","DOI":"10.1186\/1471-2350-13-123"},{"key":"e_1_2_9_6_1","doi-asserted-by":"publisher","DOI":"10.1002\/pd.911"},{"key":"e_1_2_9_7_1","doi-asserted-by":"publisher","DOI":"10.1007\/s10815-012-9783-1"},{"key":"e_1_2_9_8_1","doi-asserted-by":"publisher","DOI":"10.1007\/BF00273632"},{"key":"e_1_2_9_9_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmg.27.8.523"},{"key":"e_1_2_9_10_1","first-page":"232","article-title":"Cytogenetic investigations in 418 couples with recurrent fetal wastage","volume":"25","author":"Osztovics MK","year":"1982","journal-title":"Ann Genet"},{"key":"e_1_2_9_11_1","first-page":"243","article-title":"Trisomy 6q22 leads to 6qter due to maternal &;21 translocation. 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