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- [22] Prenatal diagnosis of familial 2q13 microduplication and a de novo Xp22.33 microdeletion in a pregnancy associated with an asymptomatic mother carrier TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2025, 64 (01): : 174 - 177
- [24] Prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, 2024, 33 (09): : 561 - 564
- [26] Interphase FISH, the structure of reciprocal translocation chromosomes and physical mapping studies rule out the duplication of the NF1 gene at 17q11.2. A reply Human Genetics, 2003, 113 : 188 - 190
- [27] Prenatal diagnosis of a familial 736-kb Xp22.2p22.13 microduplication encompassing NHS associated with an asymptomatic father carrier and no abnormality in the fetus TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2025, 64 (02): : 379 - 380
- [28] Somatic mosaicism of a > 1.7 Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH -: further evidence for a contiguous gene syndrome in 17q11.2 CYTOGENETICS AND CELL GENETICS, 1999, 85 (1-2): : 166 - 167