Nicole Morichon-Delvallez

Author PubWeight™ 7.87^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Functional disomy of the Xq28 chromosome region.	Eur J Hum Genet	2005	1.15
2	Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition.	Eur J Hum Genet	2009	0.94
3	Reproductive genetic counselling in non-mosaic 47,XXY patients: implications for preimplantation or prenatal diagnosis: Case report and review.	Hum Reprod	2003	0.87
4	Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth.	Eur J Hum Genet	2009	0.86
5	Molecular characterisation of a prenatally diagnosed 5q15q21.3 deletion and review of the literature.	Prenat Diagn	2006	0.85
6	Cytogenetic and histological features of a human embryo with homogeneous chromosome 8 trisomy.	Prenat Diagn	2006	0.82
7	Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasia.	Prenat Diagn	2008	0.81
8	Maternal uniparental heterodisomy of chromosome 17 in a patient with nephropathic cystinosis.	Eur J Hum Genet	2009	0.78
9	Molecular screening of the ZFHX1B gene in prenatally diagnosed isolated agenesis of the corpus callosum.	Prenat Diagn	2004	0.77
10	CGH analysis in a cohort of 17 chromosomally normal fetuses with an increased nuchal translucency.	Prenat Diagn	2003	0.75