The PREGCARE study: precision genetic counselling via personalised evaluation of recurrence risk for families with a child affected by a disorder caused by a de novo mutation

Abdullah UB., Bernkopf M., Koelling N., McGowan SJ., Williams J., Nemeth AH., Stewart H., Clouston P., Wilkie AOM., Goriely A.

Type

Conference paper

Publication Date

10/2019

Volume

27

Pages

1101 - 1102

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