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Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing

Clinical genetics, 2016-06, Vol.89 (6), p.659-668

2016

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Fetal phenotypes in otopalatodigital spectrum disorders

Clinical genetics, 2016-03, Vol.89 (3), p.371-377

2016

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Answer to the article by F. Vialrd et al.: Does the prevalence of recurrent pathogenic microdeletions and microdoublements in prenatal diagnosis lead to a reassessment of the evolution of non-invasive screening techniques? The example of region 22q11.2

Gynécologie, obstétrique, fertilité & sénologie, 2017-01, Vol.45 (1), p.50-53

2017

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FMR1 gene alleles in infertile women with primary ovarian insufficiency, diminished ovarian reserve and poor response to ovarian stimulation

Fertility and sterility, 2012-09, Vol.98 (3), p.S131-S132

2012

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Decreasing birth defect in children by using high magnification selected spermatozoon injection

Fertility and sterility, 2011-09, Vol.96 (3), p.S85-S85

2011

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Atypical findings in Kabuki syndrome: Report of 8 patients in a series of 20 and review of the literature

American journal of medical genetics. Part A, 2004-08, Vol.129A (1), p.64-68

2004

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Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia

Molecular human reproduction, 2016-01, Vol.22 (1), p.35-45

2016

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Perinatal outcome of 2140 singletons born from transfer of frozen-thawed embryos (FET) conceived by assisted reproductive technology (ART): a French control study 1998-2008

Fertility and sterility, 2010, Vol.94 (4), p.S241-S241

2010

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Prenatal diagnosis of a cleft of the tongue, lower lip and mandible

Ultrasound in obstetrics & gynecology, 2012-01, Vol.39 (1), p.110-112

2012

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Réponse à l’article de F. Vialard et al. : la prévalence des microdélétions et microduplications pathogènes récurrentes en diagnostic prénatal doit-elle amener à revoir l’évolution des techniques de dépistage non invasif ? L’exemple de la région 22q11.2

Gynécologie Obstétrique Fertilité & Sénologie, 2017-01, Vol.45 (1), p.50-53

2017

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Approche moléculaire de la prise en charge des immobilismes fœtaux et hypotonie néonatale

Journal de pédiatrie et de puériculture, 2003-06, Vol.16 (3), p.179-181

Viot, G.

2003

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Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies

European journal of pediatrics, 1998-11, Vol.157 (11), p.881-884

1998

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cardiopathies congénitales : quel risque pour la fratrie ?

Journal de pédiatrie et de puériculture, 2002, Vol.15 (5), p.259-264

Viot, G.

2002

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Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1

Journal of medical genetics, 2002-10, Vol.39 (10), p.714-717

2002

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Risques de morbidité maternelle et périnatale en fécondation in vitro : une étude nationale de cohorte française

Gynécologie Obstétrique Fertilité & Sénologie, 2020-04, Vol.48 (4), p.351-358

2020

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Antenatal manifestations of mitochondrial respiratory chain deficiency

The Journal of pediatrics, 2003-08, Vol.143 (2), p.208-212

2003

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SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)

Nature genetics, 1998-05, Vol.19 (1), p.67-69

1998

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Results of assisted reproductive technique in men with cystic fibrosis

Human reproduction (Oxford), 2006-05, Vol.21 (5), p.1232-1236

2006

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SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome

Acta Paediatrica, 1999-12, Vol.88 (s433), p.55-59

1999

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Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome

The Journal of pediatrics, 2001-07, Vol.139 (1), p.111-116

2001

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Constructing a fuzzy controller

Southcon/96 Conference Record, 1996, p.473-480

Viot, G.

1996

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Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome

Clinical genetics, 1998-04, Vol.53 (4), p.278-280

1998

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Deletion of chromosome 4p detected by FISH in a girl with normal high resolution karyotype

Clinical genetics, 1999-02, Vol.55 (2), p.127-129

1999

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A new case of exomphalos, short limbs, and macrogonadism syndrome

Journal of medical genetics, 2001-03, Vol.38 (3), p.e8-8

2001

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Mosaïques confinées au placenta : définition, conséquences et conduite à tenir

Journal de gynécologie obstétrique et biologie de la reproduction, 2002, Vol.31 (1), p.2S70-2S74

VIOT, G

2002

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Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing

Fetal phenotypes in otopalatodigital spectrum disorders

Answer to the article by F. Vialrd et al.: Does the prevalence of recurrent pathogenic microdeletions and microdoublements in prenatal diagnosis lead to a reassessment of the evolution of non-invasive screening techniques? The example of region 22q11.2

FMR1 gene alleles in infertile women with primary ovarian insufficiency, diminished ovarian reserve and poor response to ovarian stimulation

Decreasing birth defect in children by using high magnification selected spermatozoon injection

Atypical findings in Kabuki syndrome: Report of 8 patients in a series of 20 and review of the literature

Identification of a new DPY19L2 mutation and a better definition of DPY19L2 deletion breakpoints leading to globozoospermia

Perinatal outcome of 2140 singletons born from transfer of frozen-thawed embryos (FET) conceived by assisted reproductive technology (ART): a French control study 1998-2008

Prenatal diagnosis of a cleft of the tongue, lower lip and mandible

Réponse à l’article de F. Vialard et al. : la prévalence des microdélétions et microduplications pathogènes récurrentes en diagnostic prénatal doit-elle amener à revoir l’évolution des techniques de dépistage non invasif ? L’exemple de la région 22q11.2

Approche moléculaire de la prise en charge des immobilismes fœtaux et hypotonie néonatale

Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies

cardiopathies congénitales : quel risque pour la fratrie ?

Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1

Risques de morbidité maternelle et périnatale en fécondation in vitro : une étude nationale de cohorte française

Antenatal manifestations of mitochondrial respiratory chain deficiency

SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)

Results of assisted reproductive technique in men with cystic fibrosis

SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndrome

Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome

Constructing a fuzzy controller

Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome

Deletion of chromosome 4p detected by FISH in a girl with normal high resolution karyotype

A new case of exomphalos, short limbs, and macrogonadism syndrome

Mosaïques confinées au placenta : définition, conséquences et conduite à tenir

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