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Literature DB >> 5357204

Recurrent hydatidiform mole: a report of five cases with review of the literature.

N M Kronfol, F A Iliya, S N Hajj.

Abstract

Mesh：

Year: 1969 PMID： 5357204

Source DB: PubMed Journal: J Med Liban ISSN： 0023-9852

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8 in total

1. A strong founder effect for two NLRP7 mutations in the Indian population: an intriguing observation.

Authors: R Slim; R Bagga; W Chebaro; R Srinivasan; N Agarwal
Journal: Clin Genet Date: 2009-07-24 Impact factor: 4.438

2. Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7.

Authors: Ramesh Reddy; Elie Akoury; Ngoc Minh Phuong Nguyen; Omar A Abdul-Rahman; Christine Dery; Neerja Gupta; William P Daley; Asangla Ao; Hanene Landolsi; Rosemary Ann Fisher; Isabelle Touitou; Rima Slim
Journal: Eur J Hum Genet Date: 2012-12-12 Impact factor: 4.246

3. The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.

Authors: Ramesh Reddy; Ngoc M P Nguyen; Guillaume Sarrabay; Maryam Rezaei; Mayra C G Rivas; Aysenur Kavasoglu; Hakan Berkil; Alaa Elshafey; Ebtesam Abdalla; Kristin P Nunez; Hélène Dreyfus; Merviel Philippe; Zahra Hadipour; Asude Durmaz; Erin E Eaton; Brittany Schubert; Volkan Ulker; Fatemeh Hadipour; Fatemeh Ahmadpour; Isabelle Touitou; Majid Fardaei; Rima Slim
Journal: Eur J Hum Genet Date: 2016-03-09 Impact factor: 4.246

4. Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles.

Authors: Ngoc Minh Phuong Nguyen; Zhao-Jia Ge; Ramesh Reddy; Somayyeh Fahiminiya; Philippe Sauthier; Rashmi Bagga; Feride Iffet Sahin; Sangeetha Mahadevan; Matthew Osmond; Magali Breguet; Kurosh Rahimi; Louise Lapensee; Karine Hovanes; Radhika Srinivasan; Ignatia B Van den Veyver; Trilochan Sahoo; Asangla Ao; Jacek Majewski; Teruko Taketo; Rima Slim
Journal: Am J Hum Genet Date: 2018-11-01 Impact factor: 11.025

Recurrent hydatidiform mole: a report of five cases with review of the literature.

1. A strong founder effect for two NLRP7 mutations in the Indian population: an intriguing observation.

2. Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7.

3. The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.

4. Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles.

5. A Novel Mutation in NLRP7 Related to Recurrent Hydatidiform Mole and Reproductive Failure.

6. NLRP7 and the Genetics of Hydatidiform Moles: Recent Advances and New Challenges.

Review 7. Genetics and Epigenetics of Recurrent Hydatidiform Moles: Basic Science and Genetic Counselling.

8. Two novel mutations in the KHDC3L gene in Asian patients with recurrent hydatidiform mole.