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au.\*:("GENEVIEVE, D")

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Atypical findings in Kabuki syndrome: Report of 8 patients in a series of 20 and review of the literatureGENEVIEVE, D; AMIEL, J; VIOT, G et al.American journal of medical genetics. 2004, Vol 129A, Num 1, pp 64-68, issn 0148-7299, 5 p.Article

Clinical overlap of OFD type IX with Pallister-Killian syndrome (Tetrasomy 12p)GENEVIEVE, D; SZNAJER, Y; RAOUL, M et al.American journal of medical genetics. 2003, Vol 122A, Num 2, pp 180-182, issn 0148-7299, 3 p.Article

A CGH study of 27 patients with CHARGE associationSANLAVILLE, D; ROMANA, S. P; TURLEAU, C et al.Clinical genetics. 2002, Vol 61, Num 2, pp 135-138, issn 0009-9163Article

Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) familiesWILLEMS, M; GENEVIEVE, D; LEHEUP, B et al.Journal of medical genetics. 2010, Vol 47, Num 12, pp 797-802, issn 0022-2593, 6 p.Article

Gorlin syndrome presenting as prenatal chylothorax in a girlGENEVIEVE, D; WALTER, E; MITANCHEZ, D et al.Prenatal diagnosis. 2005, Vol 25, Num 11, pp 997-999, issn 0197-3851, 3 p.Article

Mild phenotype in a 15-year-old boy with Pallister-Killian syndromeGENEVIEVE, D; CORMIER-DAIRE, V; VEKEMANS, M et al.American journal of medical genetics. 2003, Vol 116A, Num 1, pp 90-93, issn 0148-7299, 4 p.Article

An overview of isolated and syndromic oesophageal atresiaGENEVIEVE, D; DE PONTUAL, L; AMIEL, J et al.Clinical genetics. 2007, Vol 71, Num 5, pp 392-399, issn 0009-9163, 8 p.Article

Currarino syndrome shown by prenatal onset ventriculomegaly and spinal dysraphismCRETOLLE, C; SARNACKI, S; AMIEL, J et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 8, pp 871-874, issn 1552-4825, 4 p.Article

New insights in congenital bowing of the femoraCORMIER-DAIRE, V; GENEVIEVE, D; MUNNICH, A et al.Clinical genetics. 2004, Vol 66, Num 3, pp 169-176, issn 0009-9163, 8 p.Article

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotypeFAIVRE, L; CORMIER-DAIRE, V; PRIEUR, M et al.Journal of medical genetics. 2002, Vol 39, Num 8, pp 594-596, issn 0022-2593Article

Revisiting Metatropic Dysplasia : Presentation of a Series of 19 Novel Patients and Review of the LiteratureGENEVIEVE, D; LE MERRER, M; FEINGOLD, J et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 8, pp 992-996, issn 1552-4825, 5 p.Article

A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34ISIDOR, B; DAGONEAU, N; CORMIER-DAIRE, V et al.Human genetics. 2007, Vol 121, Num 2, pp 269-273, issn 0340-6717, 5 p.Article

Long-term follow-up in a patient with metatropic dysplasia. Author's replyGENEVIEVE, D; LE MERRER, M; MUNNICH, A et al.American journal of medical genetics. 2005, Vol 135A, Num 3, pp 342-343, issn 0148-7299, 2 p.Article

Severe lactic acidosis and acute thiamin deficiency: A report of 11 neonates with unsupplemented total parenteral nutritionTHAUVIN-ROBINET, C; FAIVRE, L; SAUDUBRAY, J. M et al.Journal of inherited metabolic disease. 2004, Vol 27, Num 5, pp 700-704, issn 0141-8955, 5 p.Article

Phylogeographic consequences of different introduction histories of invasive Australian Acacia species and Paraserianthes lophantha (Fabaceae) in South AfricaLE ROUX, Johannes J; BROWN, Gillian K; BYRNE, Margaret et al.Diversity and distributions. 2011, Vol 17, Num 5, pp 861-871, issn 1366-9516, 11 p.Article

Predicting the subspecific identity of invasive species using distribution models: Acacia saligna as an exampleTHOMPSON, Genevieve D; ROBERTSON, Mark P; WEBBER, Bruce L et al.Diversity and distributions. 2011, Vol 17, Num 5, pp 1001-1014, issn 1366-9516, 14 p.Article

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