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Chromosome 21 detection in human oocyte fluorescence in situ hybridization: Possible effects...
Published in:
Journal of Assisted Reproduction & Genetics, 1998, v. 15, n. 3, p. 105, doi. 10.1023/A:1023056502731
By:
- Benzacken, B.;
- Martin-Point, B.;
- Bergé, M.;
- Hugues, J. N.;
- Wolf, J. P.;
- Selva, J.
Publication type:
Article
Assisted reproductive technology and complex chromosomal rearrangements: the limits of ICSI.
Published in:
Molecular Human Reproduction, 1997, v. 3, n. 10, p. 847, doi. 10.1093/molehr/3.10.847
By:
- Siffroi, J P;
- Benzacken, B;
- Straub, B;
- Le Bourhis, C;
- North, M O;
- Curotti, G;
- Bellec, V;
- Alvarez, S;
- Dadoune, J P
Publication type:
Article
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome.
Published in:
Clinical Genetics, 2012, v. 82, n. 2, p. 187, doi. 10.1111/j.1399-0004.2011.01697.x
By:
- Dupont, C;
- Guimiot, F;
- Perrin, L;
- Marey, I;
- Smiljkovski, D;
- Le Tessier, D;
- Lebugle, C;
- Baumann, C;
- Bourdoncle, P;
- Tabet, A-C;
- Aboura, A;
- Benzacken, B;
- Dupont, J-M
Publication type:
Article
What can we learn from old microdeletion syndromes using array-CGH screening?
Published in:
Clinical Genetics, 2012, v. 82, n. 1, p. 41, doi. 10.1111/j.1399-0004.2011.01747.x
By:
- Mosca-Boidron, A L;
- Bouquillon, S;
- Faivre, L;
- Callier, P;
- Andrieux, J;
- Marle, N;
- Bonnet, C;
- Vincent-Delorme, C;
- Berri, M;
- Plessis, G;
- Manouvrier-Hanu, S;
- Dieux-Coeslier, A;
- Thauvin-Robinet, C;
- Pipiras, E;
- Delahaye, A;
- Payet, M;
- Ragon, C;
- Masurel-Paulet, A;
- Questiaux, E;
- Benzacken, B
Publication type:
Article
Identification and characterization of a de novo partial trisomy 10p by comparative genomic hybridization (CGH).
Published in:
Clinical Genetics, 1998, v. 54, n. 4, p. 334, doi. 10.1034/j.1399-0004.1998.5440412.x
By:
- Benzacken, B.;
- Lapierre, JM;
- Siffroi, JP;
- Chalvon, A.;
- Tachdjian, G.
Publication type:
Article
Parental origin of the X-chromosome does not influence growth hormone treatment effect in Turner syndrome.
Published in:
2012
By:
- Devernay M;
- Bolca D;
- Kerdjana L;
- Aboura A;
- Gérard B;
- Tabet AC;
- Benzacken B;
- Ecosse E;
- Coste J;
- Carel JC
Publication type:
Journal Article
PRENATAL DIAGNOSIS OF ROBERTS SYNDROME: TWO NEW CASES.
Published in:
Prenatal Diagnosis, 1996, v. 16, n. 2, p. 125, doi. 10.1002/(SICI)1097-0223(199602)16:2<125::AID-PD822>3.0.CO;2-S
By:
- BENZACKEN, B.;
- SAVARY, J. B.;
- MANOUVRIER, S.;
- BUCOURT, M.;
- GONZALES, J.
Publication type:
Article
NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder.
Published in:
Clinical Genetics, 2018, v. 94, n. 2, p. 264, doi. 10.1111/cge.13383
By:
- Lévy, J.;
- Grotto, S.;
- Mignot, C.;
- Maruani, A.;
- Delahaye‐Duriez, A.;
- Benzacken, B.;
- Keren, B.;
- Haye, D.;
- Xavier, J.;
- Heulin, M.;
- Charles, E.;
- Verloes, A.;
- Dupont, C.;
- Pipiras, E.;
- Tabet, A.‐C.
Publication type:
Article
<italic>EFNB2</italic> haploinsufficiency causes a syndromic neurodevelopmental disorder.
Published in:
Clinical Genetics, 2018, v. 93, n. 6, p. 1141, doi. 10.1111/cge.13234
By:
- Lévy, J.;
- Haye, D.;
- Marziliano, N.;
- Casu, G.;
- Guimiot, F.;
- Dupont, C.;
- Teissier, N.;
- Benzacken, B.;
- Gressens, P.;
- Pipiras, E.;
- Verloes, A.;
- Tabet, A.‐C.
Publication type:
Article
Successful childbirth after intracytoplasmic morphologically selected sperm injection without assisted oocyte activation in a patient with globozoospermia.
Published in:
Human Reproduction, 2011, v. 26, n. 11, p. 2944, doi. 10.1093/humrep/der258
By:
- Sermondade, N.;
- Hafhouf, E.;
- Dupont, C.;
- Bechoua, S.;
- Palacios, C.;
- Eustache, F.;
- Poncelet, C.;
- Benzacken, B.;
- Lévy, R.;
- Sifer, C.
Publication type:
Article
Lack of submicroscopic rearrangements involving telomeres in reproductive failures.
Published in:
2002
By:
- Benzacken, B.;
- Carbillon, L.;
- Dupont, C.;
- Siffroi, J. P.;
- Monier-Gavelle, F.;
- Bucourt, M.;
- Uzan, M.;
- Wolf, J. P.
Publication type:
journal article
Familial sperm polyploidy induced by genetic spermatogenesis failure: case report.
Published in:
2001
By:
- Benzacken, Brigitte;
- Gavelle, Frédérique Monier;
- Martin-Pont, Brigitte;
- Dupuy, Olivier;
- Lièvre, Nicole;
- Hugues, Jean-Noël;
- Wolf, Jean-Philippe;
- Benzacken, B;
- Gavelle, F M;
- Martin-Pont, B;
- Dupuy, O;
- Lièvre, N;
- Hugues, J N;
- Wolf, J P
Publication type:
journal article
Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men.
Published in:
2001
By:
- Gekas, J.;
- Thepot, F.;
- Turleau, C.;
- Siffroi, J. P.;
- Dadoune, J. P.;
- Wasels, R.;
- Benzacken, B.;
- Briault, S;
- Rio, M;
- Bourouillou, G;
- Carré-Pigeon, F;
- Association des Cytogeneticiens de Langue Francaise
Publication type:
journal article
Case report. Advanced paternal age and de-novo complex chromosomal rearrangement in offspring.
Published in:
Human Reproduction, 1998, v. 13, n. 7, p. 1801, doi. 10.1093/humrep/13.7.1801
By:
- Benzacken, B;
- Siffroi, JP;
- Straub, B;
- Le Bourhis, C;
- Sauvion, S;
- Gaudelus, J;
- Dadoune, JP;
- Wolf, JP
Publication type:
Article
ARHGEF26/SGEF controls fovea formation, immunity, neurodevelopment and arteriosclerosis.
Published in:
Acta Ophthalmologica (1755375X), 2012, v. 90, p. 0, doi. 10.1111/j.1755-3768.2012.4222.x
By:
- BITOUN, P;
- PIPIRAS, E;
- BENZACKEN, B;
- DELAHAYE, A
Publication type:
Article
Prenatal BACs-on-Beads(TM) : the prospective experience of five prenatal diagnosis laboratories.
Published in:
2012
By:
- Vialard F;
- Simoni G;
- Gomes DM;
- Abourra A;
- Toffol SD;
- Bru F;
- Romero MC;
- Nitsch L;
- Bouhanna P;
- Marcato L;
- Popowski T;
- Grimi B;
- Martínez-Conejero JA;
- Benzacken B;
- Genesio R;
- Grati FR
Publication type:
Journal Article
Prenatal BACs-on-Beads<sup>TM</sup>: the prospective experience of five prenatal diagnosis laboratories.
Published in:
Prenatal Diagnosis, 2012, v. 32, n. 4, p. 329, doi. 10.1002/pd.2934
By:
- Vialard, François;
- Simoni, Giuseppe;
- Gomes, Denise Molina;
- Abourra, Azzedine;
- Toffol, Simona De;
- Bru, Fabrice;
- Romero, Maria Carmen Martinez;
- Nitsch, Lucio;
- Bouhanna, Philippe;
- Marcato, Livia;
- Popowski, Thomas;
- Grimi, Beatrice;
- Martínez-Conejero, Jose Antonio;
- Benzacken, B.;
- Genesio, Rita;
- Grati, Francesca R.
Publication type:
Article
Prenatal BACs-on-Beads([TM]) : a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis.
Published in:
2011
By:
- Vialard F;
- Simoni G;
- Aboura A;
- De Toffol S;
- Molina Gomes D;
- Marcato L;
- Serero S;
- Clement P;
- Bouhanna P;
- Rouleau E;
- Grimi B;
- Selva J;
- Gaetani E;
- Maggi F;
- Joseph A;
- Benzacken B;
- Grati FR
Publication type:
Journal Article
Prenatal BACs-on-Beads.
Published in:
Prenatal Diagnosis, 2011, v. 31, n. 5, p. 500, doi. 10.1002/pd.2727
By:
- Vialard, F.;
- Simoni, G.;
- Aboura, A.;
- De Toffol, S.;
- Molina Gomes, D.;
- Marcato, L.;
- Serero, S.;
- Clement, P.;
- Bouhanna, P.;
- Rouleau, E.;
- Grimi, B.;
- Selva, J.;
- Gaetani, E.;
- Maggi, F.;
- Joseph, A.;
- Benzacken, B.;
- Grati, F. R.
Publication type:
Article
Prenatal detection of Pierre Robin sequence with deletion Xp and additional trisomy 14q by telomere screening.
Published in:
Prenatal Diagnosis, 2007, v. 27, n. 11, p. 1062, doi. 10.1002/pd.1818
By:
- Gerard-Blanluet, M.;
- Pipiras, E.;
- Levaillant, J. M.;
- Joye, N.;
- Koubi, V.;
- Kanafani, S.;
- Vergnaud, A.;
- Verloes, A.;
- Gonzales, M.;
- Jeny, R.;
- Benzacken, B.
Publication type:
Article
Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotype.
Published in:
Prenatal Diagnosis, 2007, v. 27, n. 3, p. 279, doi. 10.1002/pd.1639
By:
- Kanafani, S.;
- Aboura, A.;
- Pipiras, E.;
- Carbillon, L.;
- Tabet, A. C.;
- Largillière, C.;
- Garel, C.;
- Gressens, P.;
- Bucourt, M.;
- Cedrin-Durnerin, I.;
- Lachassinne, E.;
- Roumegoux, C.;
- Uzan, M.;
- Hugues, J. N.;
- Wolf, J. P.;
- Benzacken, B.
Publication type:
Article
Structural chromosomal mosaicism and prenatal diagnosis.
Published in:
Prenatal Diagnosis, 2004, v. 24, n. 2, p. 101, doi. 10.1002/pd.797
By:
- E. Pipiras;
- C. Dupont;
- S. Chantot-Bastaraud;
- J. P. Siffroi;
- M. Bucourt;
- A. Batallan;
- C. Largillière;
- M. Uzan;
- J. P. Wolf;
- B. Benzacken
Publication type:
Article
De novo Subtelomeric Deletion Additional to an Inherited Apparently Balanced Reciprocal Translocation.
Published in:
Fetal Diagnosis & Therapy, 2007, v. 22, n. 4, p. 306, doi. 10.1159/000100797
By:
- Delahaye, A.;
- Pipiras, E.;
- Kanafani, S.;
- Touboul, C.;
- Vergnaud, A.;
- Encha-Razavi, F.;
- Sinico, M.;
- Benkhalifa, M.;
- Kasakyan, S.;
- Serero, S.;
- Wolf, J. P.;
- Gérard-Blanluet, M.;
- Benzacken, B.
Publication type:
Article
Unexpected inherited chromosomal translocation during prenatal diagnosis for maternal age: risk for a nondetectable karyotype imbalance in offspring.
Published in:
1998
By:
- Siffroi, Jean-Pierre;
- Heim, Nazbanou;
- Benzacken, Brigitte;
- Franco, Jean-Claude;
- Le Bourhis, Corine;
- Siffroi, J P;
- Heim, N;
- Benzacken, B;
- Franco, J C;
- Le Bourhis, C
Publication type:
journal article

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