Author/Creator: Lyonnet, S - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Lyonnet, S

1. 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisation. Issue 9 (6th January 2009)

Authors:: Malan, V; Raoul, O; Firth, H V; Royer, G; Turleau, C; Bernheim, A; Willatt, L; Munnich, A; Vekemans, M; Lyonnet, S; Cormier-Daire, V; Colleaux, L
Journal:: Journal of medical genetics
Issue:: Volume 46:Issue 9(2009)
Page Start:: 635
Record Type:: Journal Article
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2. An animal model for maternal phenylketonuria. Issue 10 (October 1991)

Authors:: Roux, C; Rey, F; Lyonnet, S; Nizard, S; Mulliez, N; Munnich, A
Journal:: Journal of medical genetics
Issue:: Volume 28:Issue 10(1991)
Page Start:: 718
Record Type:: Journal Article
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3. Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders. Issue 11 (13th July 2006)

Authors:: Jacquemont, M-L; Sanlaville, D; Redon, R; Raoul, O; Cormier-Daire, V; Lyonnet, S; Amiel, J; Le Merrer, M; Heron, D; de Blois, M-C; Prieur, M; Vekemans, M; Carter, N P; Munnich, A; Colleaux, L; Philippe, A
Journal:: Journal of medical genetics
Issue:: Volume 43:Issue 11(2006)
Page Start:: 843
Record Type:: Journal Article
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4. Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation. Issue 4 (1st April 2002)

Authors:: Rio, M; Molinari, F; Heuertz, S; Ozilou, C; Gosset, P; Raoul, O; Cormier-Daire, V; Amiel, J; Lyonnet, S; Le Merrer, M; Turleau, C; de Blois, M-C; Prieur, M; Romana, S; Vekemans, M; Munnich, A; Colleaux, L
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 4(2002)
Page Start:: 266
Record Type:: Journal Article
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5. Blepharophimosis, eczema, and growth and developmental delay in a young adult: late features of Dubowitz syndrome?. Issue 1 (January 1992)

Authors:: Lyonnet, S; Schwartz, G; Gatin, G; de Prost, Y; Munnich, A; Le Merrer, M
Journal:: Journal of medical genetics
Issue:: Volume 29:Issue 1(1992)
Page Start:: 68
Record Type:: Journal Article
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6. Conotruncal heart defects in three patients with congenital disorder of glycosylation type Ia (CDG Ia). Issue 4 (8th April 2009)

Authors:: Romano, S; Bajolle, F; Valayannopoulos, V; Lyonnet, S; Colomb, V; de Baracé, C; Vouhe, P; Pouard, P; Vuillaumier-Barrot, S; Dupré, T; de Keyzer, Y; Sidi, D; Seta, N; Bonnet, D; de Lonlay, P
Journal:: Journal of medical genetics
Issue:: Volume 46:Issue 4(2009)
Page Start:: 287
Record Type:: Journal Article
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7. Dysmorphism, variable overgrowth, normal bone age, and severe developmental delay: a "Sotos-like" syndrome?. Issue 2 (1st February 2002)

Authors:: Amiel, J; Faivre, L; Wilson, L; Le Merrer, M; Munnich, A; Winter, R; Lyonnet, S; Cormier-Daire, V
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 2(2002)
Page Start:: 148
Record Type:: Journal Article
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8. Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome. Issue 5 (30th April 2004)

Authors:: Pinson, L; Augé, J; Audollent, S; Mattéi, G; Etchevers, H; Gigarel, N; Razavi, F; Lacombe, D; Odent, S; Le Merrer, M; Amiel, J; Munnich, A; Meroni, G; Lyonnet, S; Vekemans, M; Attié-Bitach, T
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 5(2004)
Page Start:: 381
Record Type:: Journal Article
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9. Exclusion of RET and Pax 3 loci in Waardenburg-Hirschsprung disease. Issue 4 (April 1995)

Authors:: Attié, T; Till, M; Pelet, A; Edery, P; Bonnet, J P; Munnich, A; Lyonnet, S
Journal:: Journal of medical genetics
Issue:: Volume 32:Issue 4(1995)
Page Start:: 312
Record Type:: Journal Article
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10. Features of DiGeorge syndrome and CHARGE association in five patients. Issue 12 (December 1997)

Authors:: de Lonlay-Debeney, P; Cormier-Daire, V; Amiel, J; Abadie, V; Odent, S; Paupe, A; Couderc, S; Tellier, A L; Bonnet, D; Prieur, M; Vekemans, M; Munnich, A; Lyonnet, S
Journal:: Journal of medical genetics
Issue:: Volume 34:Issue 12(1997)
Page Start:: 986
Record Type:: Journal Article
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