[1] |
CHEN Xin-ying, HUANG Ting-ting, ZENG Shu-hong, JIANG Yu-ying, ZHUANG Jian-long.
Genetic Etiology Analysis of A Case of Fetal Lymphedema
[J]. Journal of International Reproductive Health/Family Planning, 2024, 43(5): 395-398.
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[2] |
FU Wan-yu, JIN Sha-wen, JIANG Yu-ying, LI Yan-qing.
Clinical Effect of Noninvasive Prenatal Screening Techniques for Rare Autosomal Trisomies and Chromosome Copy Number Variation
[J]. Journal of International Reproductive Health/Family Planning, 2024, 43(4): 279-283.
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[3] |
LIU Guo-zhong, HOU Hai-yan, CHANG Yu, HAO Chun-xia, SUI Li-ting.
Genetic Analysis of Second Pregnancy with A Child of 21-Trisomy Syndrome in A Phenotypically Normal Mother
[J]. Journal of International Reproductive Health/Family Planning, 2024, 43(4): 305-308.
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[4] |
CHEN Chun, DENG Guang-ming, CHEN Xi-min, WANG Jin, CHENG De-hua, QIN Sheng-fang, SONG Xiao.
Genetic Analysis of A Fetus with Chromosomal Abnormalities Caused by Sperm Generated by Adjacent-2 Segregation
[J]. Journal of International Reproductive Health/Family Planning, 2024, 43(3): 195-200.
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[5] |
ZHUANG Jian-long, JIANG Yu-ying, ZENG Shu-hong, CHEN Xin-ying.
Genetic Analysis of A Family with Recurrent Spontaneous Abortion Using FISH Combined with Chromosome Karyotype
[J]. Journal of International Reproductive Health/Family Planning, 2024, 43(3): 201-203.
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[6] |
LI Yan-qing, FU Wan-yu, CHEN Geng-bo, WANG Yuan-bai, JIANG Yu-ying, XIAO Shan-shan, ZHUANG Jian-long.
Prenatal Diagnosis of 22q11 Microdeletion Syndrome in 11 Fetuses
[J]. Journal of International Reproductive Health/Family Planning, 2023, 42(2): 115-118.
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[7] |
LI Yan-qing, SU Jing-ming, CHEN Geng-bo, JIANG Yu-ying, WANG Yuan-bai, XIAO Shan-shan, ZHUANG Jian-long.
Prenatal Diagnosis and Clinical Genetic Analysis of Chromosome 22q11.2 Microduplications
[J]. Journal of International Reproductive Health/Family Planning, 2023, 42(1): 23-26.
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[8] |
LI Yan-qing, FU Wan-yu, WU Su-xia, JIANG Yu-ying, WANG Yuan-bai, ZHUANG Jian-long.
A Case of 17p13.3p13.2 Microdeletion Fetus and Literature Review
[J]. Journal of International Reproductive Health/Family Planning, 2022, 41(5): 389-392.
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[9] |
PEI Jiao-jiao, XIE Jiang-yan, WU Xiao-li.
Polymorphism of Folic Acid Carrier Gene and Fetal Neural Tube Malformation
[J]. Journal of International Reproductive Health/Family Planning, 2021, 40(6): 519-523.
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[10] |
CHEN Xiao-jun, JIA Yu-sen, ZHANG Zhi-jie.
Protamine and Teratozoospermia: A Short Review
[J]. Journal of International Reproductive Health/Family Planning, 2021, 40(3): 216-220.
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[11] |
MA Li-na, MA Hong-li, GAO Jing-shu, WU Xiao-ke.
Candidate Genes Related to Polycystic Ovary Syndrome
[J]. Journal of International Reproductive Health/Family Planning, 2021, 40(2): 153-156.
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[12] |
CHEN Hai-xia, BAI Xiao-hong.
Advances in Molecular Genetics of Diminished Ovarian Reserve
[J]. Journal of International Reproductive Health/Family Planning, 2020, 39(5): 411-415.
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[13] |
CAI Chan-hui, LI Yi, HU Jing-jing, LI Xing, LI Xian-zheng.
Clinical Genetic Characteristics of Imbalanced Translocation between Xp/Yq Chromosomes
[J]. Journal of International Reproductive Health/Family Planning, 2020, 39(3): 202-206.
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[14] |
MENG Ye,TAO Yuan-yuan,HU Xin,SANG Mei-ying,TONG Xian-hong.
Screening of Common Deafness Gene Mutations in 129 Children Conceived through Assisted Reproductive Technology
[J]. Journal of International Reproductive Health/Family Planning, 2020, 39(2): 113-116.
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[15] |
LI Xian-zheng,XU Ling,HU Jing-jing,LI Feng-zhen,CAI Chan-hui.
Application of Fluorescence in situ Hybridization in Prenatal Diagnosis of Chromosomal Mosaicism
[J]. Journal of International Reproductive Health/Family Planning, 2020, 39(2): 104-108.
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