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Assessment of biphasic CAPA-IVM for improving equine oocyte quality and developmental potential
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- Miscellaneous
- open access
Non-coding structural variants identify a commonly affected regulatory region steering FOXG1 transcription in early neurodevelopment
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- Journal Article
- A2
- open access
Exploring aneuploidies in two-center isolated bovine embryonic stem cell lines : implications for cultured meat production
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RNA-sequencing unveils FLT4 splice site variants in variable congenital heart disease
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- Journal Article
- A1
- open access
Pronuclear transfer rescues poor embryo development of in vitro-grown secondary mouse follicles
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Implicit bias in diagnosing mosaicism amongst preimplantation genetic testing providers : results from a multicenter study of 36 395 blastocysts
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Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability
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Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder
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Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder
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Structural variants disrupt a critical regulatory region downstream of FOXG1