Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

EMMA Martin, A Enriquez, DB Sparrow… - Human molecular …, 2020 - academic.oup.com
The genetic causes of multiple congenital anomalies are incompletely understood. Here, we
report novel heterozygous predicted loss-of-function (LoF) and predicted damaging …
被引用次数：18 相关文章

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

EMMA Martin, A Enriquez, DB Sparrow… - Human Molecular …, 2020 - academic.oup.com
The genetic causes of multiple congenital anomalies are incompletely understood. Here, we
report novel heterozygous predicted loss-of-function (LoF) and predicted damaging …

[引用][C] Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

EMMA Martin, A Enriquez… - Human Molecular …, 2020 - espace.library.uq.edu.au
The genetic causes of multiple congenital anomalies are incompletely understood. Here, we
report novel heterozygous predicted loss-of-function (LoF) and predicted damaging …

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

EMMA Martin, A Enriquez, DB Sparrow… - Human molecular …, 2020 - pure.johnshopkins.edu
The genetic causes of multiple congenital anomalies are incompletely understood. Here, we
report novel heterozygous predicted loss-of-function (LoF) and predicted damaging …
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[HTML][HTML] Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

EMMA Martin, A Enriquez, DB Sparrow… - Human Molecular …, 2020 - ncbi.nlm.nih.gov
The genetic causes of multiple congenital anomalies are incompletely understood. Here, we
report novel heterozygous predicted loss-of-function (LoF) and predicted damaging …

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.

E Martin, A Enriquez, DB Sparrow… - Human Molecular …, 2020 - europepmc.org
The genetic causes of multiple congenital anomalies are incompletely understood. Here, we
report novel heterozygous predicted loss-of-function (LoF) and predicted damaging …

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

EMMA Martin, A Enriquez… - Human Molecular …, 2020 - eprints.victorchang.edu.au
The genetic causes of multiple congenital anomalies are incompletely understood. Here, we
report novel heterozygous predicted loss-of-function (LoF) and predicted damaging …

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.

EMMA Martin, A Enriquez, DB Sparrow… - Human Molecular …, 2020 - search.ebscohost.com
The genetic causes of multiple congenital anomalies are incompletely understood. Here, we
report novel heterozygous predicted loss-of-function (LoF) and predicted damaging …

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

EMMA Martin, A Enriquez… - Human molecular …, 2020 - pubmed.ncbi.nlm.nih.gov
The genetic causes of multiple congenital anomalies are incompletely understood. Here, we
report novel heterozygous predicted loss-of-function (LoF) and predicted damaging …

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

EMMA Martin, A Enriquez, DB Sparrow… - Human Molecular …, 2020 - kclpure.kcl.ac.uk
The genetic causes of multiple congenital anomalies are incompletely understood. Here, we
report novel heterozygous predicted loss-of-function (LoF) and predicted damaging …