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E Westenius^{1

2}, E Sahlin^{1

2}, P Conner^{3

4}, A Lindstrand^{1

2}, E Iwarsson^{1

2}

Affiliations

¹ Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
² Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
³ Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
⁴ Centre for Fetal Medicine, Karolinska University Hospital, Stockholm, Sweden.

Free article

Comment

E Westenius et al. Ultrasound Obstet Gynecol. 2022 Oct.

Free article

. 2022 Oct;60(4):586.

doi: 10.1002/uog.26064.

E Westenius^{1

2}, E Sahlin^{1

2}, P Conner^{3

4}, A Lindstrand^{1

2}, E Iwarsson^{1

2}

¹ Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
² Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.
³ Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
⁴ Centre for Fetal Medicine, Karolinska University Hospital, Stockholm, Sweden.

No abstract available

Comment on

Prenatal diagnosis of non-immune hydrops fetalis: whole-exome sequencing or whole-genome sequencing?
Lin XM, Li DZ. Lin XM, et al. Ultrasound Obstet Gynecol. 2022 Oct;60(4):585-586. doi: 10.1002/uog.26063. Ultrasound Obstet Gynecol. 2022. PMID: 36183347 No abstract available.

1. Westenius E, Sahlin E, Conner P, Lindstrand A, Iwarsson E. Diagnostic yield using whole-genome sequencing and in-silico panel of 281 genes associated with non-immune hydrops fetalis in clinical setting. Ultrasound Obstet Gynecol 2022; 60: 487-493.
1. Stranneheim H, Lagerstedt-Robinson K, Magnusson M, Kvarnung M, Nilsson D, Lesko N, Engvall M, Anderlid BM, Arnell H, Johansson CB, Barbaro M, Björck E et al. Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients. Genome Med 2021; 13: 40.