Biallelic TMEM260 variants cause truncus arteriosus, with or without renal defects von Pagnamenta, Alistair T., Jackson, Adam, Perveen, Rahat, Beaman, Glenda, Petts, Gemma, Gupta, Asheeta, Hyder, Zerin, Chung, Brian Hon‐Yin, Kan, Anita Sik‐Yau, Cheung, Ka Wang, Kerstjens‐Frederikse, Wilhelmina S., Abbott, Kristin M., Elpeleg, Orly, Taylor, Jenny C., Banka, Siddharth, Ta‐Shma, Asaf

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Prenatal and postnatal diagnosis of Schuurs‐Hoeijmakers syndrome: Case series and review of the literature von Seto, Mimi Tin‐Yan, Bertoli‐Avella, Aida M., Cheung, Ka Wang, Chan, Kelvin Yuen‐Kwong, Yeung, Kit San, Fung, Jasmine Lee‐Fong, Beetz, Christian, Bauer, Peter, Luk, Ho Ming, Lo, Ivan Fai‐Man, Lee, Chin Peng, Chung, Brian Hon‐Yin, Kan, Anita Sik‐Yau

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Exome sequencing identifies molecular diagnosis in children with drug‐resistant epilepsy von Tsang, Mandy Ho‐Yin, Leung, Gordon Ka‐Chun, Ho, Alvin Chi‐Chung, Yeung, Kit‐San, Mak, Christopher Chun‐Yu, Pei, Steven Lim‐Cho, Yu, Mullin Ho‐Chung, Kan, Anita Sik‐Yau, Chan, Kelvin Yuen‐Kwong, Kwong, Karen Ling, Lee, So‐Lun, Yung, Ada Wing‐Yan, Fung, Cheuk‐Wing, Chung, Brian Hon‐Yin

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Expanded Carrier Screening in Chinese Population - A Survey on Views and Acceptance of Pregnant and Non-Pregnant Women von Cheng, Hiu Yee Heidi, Wong, Grace Ching Yin, Chan, Yuen-Kwong Kelvin, Lee, Chin Peng, Tang, Mary Hoi Yin, Ng, Ernest Hung-Yu, Kan, Anita Sik-Yau

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Parental decisions following prenatal diagnosis of sex chromosome aneuploidy in Hong Kong von So, Po Lam, Cheng, Kwun Yue Yvonne, Cheuk, Kwan Yiu, Chiu, Wan Kam, Mak, Shui Lam, Mok, Sau Lan, Lo, Tsz Kin, Yung, Wai Kuen, Lo, Fai Man, Chung, Hon Yin Brian, Kan, Sik Yau Anita, Lee, Chin Peng, Tang, Hoi Yin Mary

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Informed choice and decision making in women offered cell‐free DNA prenatal genetic screening von Lo, Tsz‐Kin, Chan, Kelvin Yuen‐Kwong, Kan, Anita Sik‐Yau, So, Po‐Lam, Kong, Choi‐Wah, Mak, Shui‐Lam, Lee, Chung‐Nin

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A Fetus with Congenital Microcephaly, Microphthalmia and Cataract Was Detected with Biallelic Variants in the OCLN Gene: A Case Report von Ng, Vivian Kwun Sin, Lau, Tze Kin, Kan, Anita Sik Yau, Chung, Brian Hon Yin, Luk, Ho Ming, Ng, Wai Fu, Shi, Mengmeng, Choy, Kwong Wai, Cao, Ye, Leung, Wing Cheong

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Study of the extent of information desired by women undergoing non‐invasive prenatal testing following positive prenatal Down‐syndrome screening test results von Lo, Tsz‐Kin, Chan, Kelvin Yuen‐Kwong, Kan, Anita Sik‐Yau, So, Po‐Lam, Kong, Choi‐Wah, Mak, Shui‐Lam, Lee, Chung‐Nin

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Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese von Chau, Jeffrey Fong Ting, Yu, Mullin Ho Chung, Chui, Martin Man Chun, Yeung, Cyrus Chun Wing, Kwok, Aaron Wing Cheung, Zhuang, Xuehan, Lee, Ryan, Fung, Jasmine Lee Fong, Lee, Mianne, Mak, Christopher Chun Yu, Ng, Nicole Ying Ting, Chung, Claudia Ching Yan, Chan, Marcus Chun Yin, Tsang, Mandy Ho Yin, Chan, Joshua Chun Ki, Chan, Kelvin Yuen Kwong, Kan, Anita Sik Yau, Chung, Patrick Ho Yu, Yang, Wanling, Lee, So Lun, Chan, Godfrey Chi Fung, Tam, Paul Kwong Hang, Lau, Yu Lung, Yeung, Kit San, Chung, Brian Hon Yin, Tang, Clara Sze Man

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A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin von Kan, Anita Sik Yau, Lau, Elizabeth Tak Kwong, So, Chun Hong, Chan, Wan Pang, Wong, Wing Cheuk, Lee, Kam Cheong, Pertile, Mark D., Tang, Mary Hoi Yin

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Prenatal diagnosis and long‐term follow‐up of a Chinese patient with mosaic variegated aneuploidy and its molecular analysis von Lin, Sheng Mou, Luk, Ho Ming, Lo, Ivan Fai Man, Tam, Wai‐Keung, Chan, Kelvin Yuen Kwong, Tse, Hei‐Yee, Leung, Wing Cheong, Tang, Mary Hoi Yin, Kan, Anita Sik Yau

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Prenatal diagnosis of Myhre syndrome with a heterozygous pathogenic variant in SMAD4 gene presented with thick nuchal translucency and cardiac abnormalities von Hui, Pui Wah, Mok, Yin Kwan, Luk, Ho Ming, Au, Sandy Leung Kuen, Lau, Eunice Yuen Ting, Chung, Brian, Kan, Anita Sik Yau

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Pregnancy-associated plasma protein A for prediction of fetal growth restriction von Lo, Tsz-kin, Chan, Kelvin Yuen-kwong, Chan, Sario Sau-yuk, Kan, Anita Sik-yau, Hui, Amelia Pui-wah, Tang, Mary Hoi-yin

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Genetic Counseling/Consultation in South-East Asia: A Report from the Workshop at the 10th Asia Pacific Conference on Human Genetics von Zayts, Olga, Sarangi, Srikant, Thong, Meow-Keong, Chung, Brian Hon-yin, Lo, Ivan Fao-man, Kan, Anita Sik-yau, Lee, Juliana Mei-Har, Padilla, Carmencita David, Cutiongco-de la Paz, Eva Maria, Faradz, Sultana M. H., Wasant, Pornswan

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Antenatal counselling of congenital surgical anomalies: A decade of experience in a local tertiary centre von Fung, Adrian Chi Heng, Kan, Anita Sik Yau, Chung, Patrick HY, Shek, Noel Wing Man, Chan, Ivy Hau Yee, Wong, Kenneth Kak Yuen

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Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies von So, Po Lam, Hui, Annie Shuk Yi, Ma, Teresa Wei Ling, Shu, Wendy, Hui, Amelia Pui Wah, Kong, Choi Wah, Lo, Tsz Kin, Kan, Amanda Nim Chi, Kan, Elaine Yee Ling, Chong, Shuk Ching, Chung, Brian Hon Yin, Luk, Ho Ming, Choy, Kwong Wai, Kan, Anita Sik Yau, Leung, Wing Cheong

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A case of prenatal isolated talipes and 22q11.2 deletion syndrome—an important chromosomal disorder missed by noninvasive prenatal screening von Cheung, Ka Wang, Lai, Carman Wing Sze, Mak, Christopher Chun Yu, Hui, Pui Wah, Chung, Brian Hon Yin, Kan, Anita Sik Yau

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Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong von Chung, Claudia Ching Yan, Chan, Kelvin Yuen Kwong, Hui, Pui Wah, Au, Patrick Kwok Cheung, Tam, Wai Keung, Li, Samuel Kai Man, Leung, Gordon Ka Chun, Fung, Jasmine Lee Fong, Chan, Marcus Chun Yin, Luk, Ho Ming, Mak, Annisa Shui Lam, Leung, Kwok Yin, Tang, Mary Hoi Yin, Chung, Brian Hon Yin, Kan, Anita Sik Yau

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Evaluating the Clinical Utility of Genome Sequencing for Cytogenetically Balanced Chromosomal Abnormalities in Prenatal Diagnosis von Yu, Mullin Ho Chung, Chau, Jeffrey Fong Ting, Au, Sandy Leung Kuen, Lo, Hei Man, Yeung, Kit San, Fung, Jasmine Lee Fong, Mak, Christopher Chun Yu, Chung, Claudia Ching Yan, Chan, Kelvin Yuen Kwong, Chung, Brian Hon Yin, Kan, Anita Sik Yau

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Bridging the gap from prenatal karyotyping to whole-genome array comparative genomic hybridization in Hong Kong: survey on knowledge and acceptance of health-care providers and pre... von Cheng, Hiu Yee Heidi, Kan, Anita Sik-yau, Hui, Pui Wah, Lee, Chin Peng, Tang, Mary Hoi Yin

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