L. Taine

F. Moreau-Gaudry, J. Reiffers, J. D. Di Santo, 1999, Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research.

Molecular characterization of an 11q14.3 microdeletion associated with leukodystrophy

C. Rooryck, D. Lacombe, L. Taine, 2004, European Journal of Human Genetics.

Neoplastic Cells Do Not Carry bcl2-JH Rearrangements Detected in a Subset of Primary Cutaneous Follicle Center B-cell Lymphomas

P. Dubus, J. Merlio, M. Beylot-Barry, 2004, The American journal of surgical pathology.

Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia type B (IND B)

M. Vidaud, I. Laurendeau, D. Vidaud, 2000, Journal of medical genetics.

A YAC contig encompassing the 11q14.3 breakpoint of a translocation associated with schizophrenia, and including the tyrosinase gene

L. Taine, B. Arveiler, P. Boisseau, 1999, Mammalian Genome.

Identification of a complex 17q rearrangement in a metanephric stromal tumor.

J. Toutain, L. Taine, M. Doco‐Fenzy, 2011, Cancer genetics.

Effective gene therapy of mice with congenital erythropoietic porphyria is facilitated by a survival advantage of corrected erythroid cells.

I. Lamrissi‐Garcia, M. Lalanne, C. Ged, 2008, American journal of human genetics.

Combination of WAGR and Potocki–Shaffer contiguous deletion syndromes in a patient with an 11p11.2–p14 deletion

J. Crolla, A. Verloes, D. Lacombe, 2005, European Journal of Human Genetics.

Successful therapeutic effect in a mouse model of erythropoietic protoporphyria by partial genetic correction and fluorescence-based selection of hematopoietic cells

C. Ged, E. Richard, F. Moreau-Gaudry, 2001, Gene Therapy.

Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH.

M. Bouvard, D. Lacombe, L. Taine, 2000, American journal of medical genetics.

Is non‐echogenic nuchal oedema a marker in trisomy 21 screening?

L. Taine, R. Saura, J. Horovitz, 1994, Prenatal diagnosis.

Chromosome analysis of adenomatous polyps of the colon: possible existence of two differently evolving cytogenetic groups.

P. Couzigou, L. Taine, F. Dumas, 1993, Cancer genetics and cytogenetics.

High-resolution integrated map encompassing the breast cancer loss of heterozygosity region on human chromosome 16q22.1.

P. Rocca-Serra, H. Prydz, L. Taine, 2000, Genomics.

The CAG repeat within the androgen receptor gene in male breast cancer patients

B. Assouline, I. Laurendeau, S. Lyonnet, 2000, Journal of medical genetics.

False‐negative results of trisomy 21 on direct analysis on chorionic villus sampling

L. Taine, R. Saura, J. Horovitz, 1998, Prenatal diagnosis.

Prenatal diagnosis of trisomy 9. Six cases and a review of the literature

L. Taine, R. Saura, J. Horovitz, 1995, Prenatal diagnosis.

12th Fetal Cell Workshop

P. Hufnagl, J. Foidart, M. Dietel, 2001, Fetal Diagnosis and Therapy.

Analysis of CBP (CREBBP) gene deletions in Rubinstein‐Taybi syndrome patients using real‐time quantitative PCR

D. Lacombe, L. Monnet, L. Taine, 2004, Human mutation.

Confirmation of assignment of a locus for Rubinstein-Taybi syndrome gene to 16p13.3.

D. Lacombe, L. Taine, R. Saura, 1992, American journal of medical genetics.

An unusual chromosome 22q11 deletion associated with an apparent complementary ring chromosome in a phenotypically normal woman.

J. Toutain, D. Lacombe, L. Taine, 2011, European journal of medical genetics.

Characterization of a de novo balanced translocation t(9;18)(p23;q12.2) in a patient with oculoauriculovertebral spectrum.

C. Rooryck, D. Lacombe, L. Taine, 2010, European journal of medical genetics.

Pregnancy Outcome and Prognosisin Fetuses with Increased First-TrimesterNuchal Translucency

F. Guyon, L. Taine, R. Saura, 2001, Fetal Diagnosis and Therapy.

Mapping, characterization, and expression analysis of the SM-20 human homologue, c1orf12, and identification of a novel related gene, SCAND2.

B. Bloch, D. Dupuy, I. Aubert, 2000, Genomics.

PRENATAL DIAGNOSIS IN CONGENITAL ERYTHROPOIETIC PORPHYRIA BY METABOLIC MEASUREMENT AND DNA MUTATION ANALYSIS

P. Calvas, C. Ged, F. Moreau-Gaudry, 1996, Prenatal diagnosis.

Reversion of hepatobiliary alterations by bone marrow transplantation in a murine model of erythropoietic protoporphyria

X. Montagutelli, A. Fontanellas, F. Mazurier, 2000, Hepatology.

Feasibility, accuracy and safety of chorionic villus sampling: a report of 10 741 cases

F. Guyon, L. Taine, R. Saura, 2003, Prenatal diagnosis.

Evaluation of chorion villus sampling

L. Taine, R. Saura, J. Horovitz, 1991, The Lancet.

18p monosomy with midline defects and a de novo satellite identified by FISH.

D. Lacombe, L. Taine, C. Goizet, 1997, Annales de genetique.

Operator experience and fetal loss rate in transabdominal CVS

L. Taine, R. Saura, J. Horovitz, 1994, Prenatal diagnosis.

Risks of transabdominal chorionic villus sampling before the 12th week of amenorrhea

L. Taine, M. Longy, R. Saura, 1990, Prenatal diagnosis.

A modified freehand ultrasonographically guided technique in transabdominal chorionic villus sampling.

L. Taine, R. Saura, J. Horovitz, 1992, American journal of obstetrics and gynecology.

Why confine chorionic villus biopsy to single pregnancies?

L. Taine, R. Saura, J. Horovitz, 1993, Prenatal Diagnosis.

A simple method of chromosomal analysis for malignant solid tumors.

L. Taine, M. Longy, R. Saura, 1992, Cancer genetics and cytogenetics.

Prenatal diagnosis and management of sex chromosome aneuploidy: a report on 98 cases

L. Taine, R. Saura, J. Horovitz, 2004, Prenatal diagnosis.

Trisomy 22 with thyroid isthmus agenesis and absent gall bladder.

D. Lacombe, L. Taine, R. Saura, 2004, Genetic Counseling.

Abdominal lymphatic dysplasia and 22q11 microdeletion.

B. le Bail, D. Lacombe, L. Taine, 1999, Genetic counseling.

Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.

S. Knight, C. Stoll, J. Mandel, 1996, American journal of human genetics.

[Prenatal diagnosis of nuchal edemas and cystic hygromas of the neck. 49 cases].

L. Taine, R. Saura, J. Horovitz, 1995, Journal de gynecologie, obstetrique et biologie de la reproduction.

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations

P. Fergelot, J. Toutain, D. Lacombe, 2019, Clinical genetics.

A review of malignancies in fragile X syndrome and report of an Ewing sarcoma

B. Bui, D. Lacombe, M. Vekemans, 2008 .

A 580 kb microdeletion in 17q21.32 associated with mental retardation, microcephaly, cleft palate, and cardiac malformation.

C. Rooryck, D. Lacombe, L. Taine, 2008, European journal of medical genetics.

Refined localisation of the voltage-gated chloride channel, CLCN3, to 4q33

D. Lacombe, L. Taine, B. Arveiler, 1998, Human Genetics.

[Acquired astigmatism caused by chalazion].

L. Taine, M. Corbel, R. Asseman, 1965, Bulletin des societes d'ophtalmologie de France.

A novel mutation and novel features in Nijmegen breakage syndrome

A. Green, E. Shoubridge, A. Munnich, 2001, Journal of medical genetics.

Proportion of Parents Agreeing to Delay Fetal Karyotyping until the Third Trimester of Pregnancy in Cases with an Indication

J. Toutain, L. Taine, R. Saura, 2012, Fetal Diagnosis and Therapy.

EcoRl Blots Used for FRAXA Diagnosis: Analysis of Four FRAXE Families with Mild Mental Retardation in Males

S. Knight, D. Lacombe, V. Biancalana, 2007 .

Molecular analysis of the CBP gene in 60 patients with Rubinstein-Taybi syndrome

C. Cruaud, D. Lacombe, L. Taine, 2002, Journal of medical genetics.