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	1	10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in France Enthalten in Orphanet journal of rare diseases Bd. 16, 4.8.2021, Nr. 1, date:12.2021: 1-14
	2	A framework to identify contributing genes in patients with Phelan-McDermid syndrome Enthalten in npj Genomic Medicine Bd. 2, 23.10.2017, Nr. 1, date:12.2017: 1-9
	3	Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome Enthalten in npj Genomic Medicine Bd. 4, 1.7.2019, Nr. 1, date:12.2019: 1
	4	Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation Enthalten in Breast cancer research Bd. 23, 3.8.2021, Nr. 1, date:12.2021: 1-18
	5	GENESIS: a French national resource to study the missing heritability of breast cancer Enthalten in BMC cancer Bd. 16, 12.1.2016, Nr. 1, date:12.2016: 1-9
	6	Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors Enthalten in Nature Communications Bd. 15, 10.9.2024, Nr. 1, date:12.2024: 1-18

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