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- [22] Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12) AMERICAN JOURNAL OF MEDICAL GENETICS, 2000, 92 (05): : 328 - 335
- [24] Prenatal diagnosis of the maternal derivative chromosome der(15) t(Y;15)(q12;p13) in a dizygotic twin pregnancy TZU CHI MEDICAL JOURNAL, 2016, 28 (04): : 176 - 179
- [26] Isolated familial somatotropinomas: Establishment of linkage to chromosome 11q13.1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12 JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (02): : 707 - 714
- [27] Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2018, 57 (05): : 734 - 738
- [28] Incidental detection of familial 8p23.2 microduplication encompassing CSMD1 associated with mosaic 46,XY,t(7;8)(q31.2;p23.1)/46,XY at amniocentesis in a pregnancy with no apparent phenotypic abnormality and a favorable outcome TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2024, 63 (02): : 245 - 249
- [29] Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2015, 54 (06): : 797 - 798
- [30] Report Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2021, 60 (04): : 775 - 777