Pathogenic variant in NLRP7 (19q13.42) associated with recurrent gestational trophoblastic disease: Data from early embryo development observed during in vitro fertilization-Reference-Cited by-同舟云学术

Pathogenic variant in NLRP7 (19q13.42) associated with recurrent gestational trophoblastic disease: Data from early embryo development observed during in vitro fertilization

Published:2017 Issue:1 Volume:44 Page:40
ISSN:2233-8233
Container-title:Clinical and Experimental Reproductive Medicine
language:en
Short-container-title:Clin Exp Reprod Med

Author:

Sills E. Scott¹²,Obregon-Tito Alexandra J.³,Gao Harry³,McWilliams Thomas K.⁴,Gordon Anthony T.⁴,Adams Catharine A.⁵,Slim Rima⁶

Affiliation:

1. Reproductive Research Section, Center for Advanced Genetics, Carlsbad, CA, USA.

2. Department of Obstetrics and Gynecology, Palomar Medical Center, Escondido, CA, USA.

3. Fulgent Diagnostics, Temple City, CA, USA.

4. Genesis Genetics Inc., Plymouth, MI, USA.

5. Reproductive Sciences Medical Center, San Diego, CA, USA.

6. Department of Human Genetics, McGill University Health Centre Research Institute, Montréal, QC, Canada.

Publisher

The Korean Society for Reproductive Medicine

Subject

Reproductive Medicine

Link

https://synapse.koreamed.org/pdf/10.5653/cerm.2017.44.1.40

Reference22 articles.

1. The genetics of gestational trophoblastic disease: a rare complication of pregnancy

2. A global disorder of imprinting in the human female germ line

3. Recurrent hydatidiform mole: A case report of six consecutive molar pregnancies complicated by choriocarcinoma, and review of the literature

4. Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte

5. Mutations inNLRP7are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles

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