Preimplantation genetic risk reduction: a new dilemma in the era of chromosomal microarrays and exome sequencing
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Reproductive Medicine,Obstetrics and Gynecology
Reference17 articles.
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2. Preimplantation genetic diagnosis (PGD) for nonsyndromic deafness by polar body and blastomere biopsy;Altarescu;J. Assist. Reprod. Genet,2009
3. Parent of origin, mosaicism, and recurrence risk: probabilistic modeling explains the broken symmetry of transmission genetics;Campbell;Am. J. Hum. Genet,2014
4. Decision-making on preimplantation genetic diagnosis and prenatal diagnosis: a challenge for couples with hereditary breast and ovarian cancer;Derks-Smeets;Hum. Reprod,2014
5. Human MutL homolog (MLH1) function in DNA mismatch repair: a prospective screen for missense mutations in the ATPase domain;Ellison;Nucleic Acids Res,2004
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5. Thirteen years' experience of 893 PGD cycles for monogenic disorders in a publicly funded, nationally regulated regional hospital service;Reproductive BioMedicine Online;2018-02
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