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Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region

American journal of human genetics, 1995-07, Vol.57 (1), p.62-71

1995

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An ovarian dysgerminoma in Down syndrome. Hypothesis about the association

International journal of gynecological cancer, 2006-02, Vol.16 (S1), p.375-379

2006

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De novo complex chromosomal rearrangements (CCR) involving chromosome 1, 5, and 6 resulting in microdeletion for 6q14 in a female carrier with psychotic disorder

American journal of medical genetics, 2004-07, Vol.128A (2), p.199-203

2004

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No significant effect of monosomy for distal 21q22.3 on the down syndrome phenotype in Mirror duplications of chromosome 21

American journal of human genetics, 1992-12, Vol.51 (6), p.1240-1250

1992

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The 50th anniversary of the discovery of trisomy 21: The past, present, and future of research and treatment of Down syndrome

Genetics in medicine, 2009-09, Vol.11 (9), p.611-616

2009

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Eleven new cases of del(9p) and features from 80 cases

Journal of medical genetics, 1988-11, Vol.25 (11), p.741-749

1988

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Métabolisme des substrats monocarbonés et trisomie 21: analyse de l'impact des polymorphismes génétiques

Annales de biologie clinique (Paris), 2002-11, Vol.60 (6), p.647-653

2002

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ETUDE DE LA DESCENDANCE DE SUJETS TRAITÉS PAR RADIOTHÉRAPIE PELVIENNE

Human heredity, 2008-08, Vol.6 (2), p.204-216

2008

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Les dysmorphies liées aux aberrations chromosomiques autosomiques de l'enfant à l'adulte

Bulletin de l'Académie nationale de médecine, 1989-11, Vol.173 (8), p.1093-1101

RETHORE, M.-O

1989

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Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13

Cytogenetic and genome research, 1989, Vol.50 (2-3), p.70-74

1989

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Surrogate pregnancy with regard to marriage between persons of the same sex

Bulletin de l'Académie nationale de médecine, 2014-04, Vol.198 (4-5), p.917-950

Henrion, Roger

2014

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Cystathionine beta synthase: Gene dosage effect in trisomy 21

Biochemical and biophysical research communications, 1985-04, Vol.128 (1), p.40-44

1985

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DNA polymorphism analysis in families with recurrence of free trisomy 21

American journal of human genetics, 1992-11, Vol.51 (5), p.1015-1027

1992

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Differences in purine metabolism in patients with Down's syndrome

Journal of intellectual disability research, 1993-12, Vol.37 (6), p.491-505

1993

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Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene

Human genetics, 1998-02, Vol.102 (2), p.151-156

1998

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In vivo folic acid supplementation partially corrects in vitro methotrexate toxicity in patients with Down syndrome

British journal of haematology, 1995-03, Vol.89 (3), p.678-680

1995

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The child and his family

Soins. Gynecologie, obstetrique, puericulture, pediatrie, 1992-06 (133-134), p.25

Rethoré, M O

1992

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An ovarian dysgerminoma in Down syndrome. Hypothesis about the association

International journal of gynecological cancer, 2006-01, Vol.16 (Suppl 1), p.375-379

2006

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Consequences of the effects of gene determinations

Annales de biologie clinique (Paris), 1974, Vol.32 (3), p.291

Rethoré, M O

1974

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A 23-year-old woman with down syndrome, type 1 neurofibromatosis, and breast carcinoma

American journal of medical genetics, 2004-02, Vol.125A (1), p.94-96

2004

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Excessive glutamine sensitivity in Alzheimer's disease and Down syndrome lymphocytes

Journal of the neurological sciences, 1995-11, Vol.133 (1), p.31-41

1995

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Announcement of diagnosis of 21-trisomy and abandonment

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 1994-09, Vol.1 (9), p.856

1994

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Structural variation of chromosome 21 and symptoms of Down's syndrome

Human genetics. Supplement, 1981, Vol.2, p.173

Rethoré, M O

1981

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Analyse du caryotype dePan paniscus. Comparaison avec les autresPongidae etl'Homme

Human genetics, 1975-06, Vol.28 (2), p.113-119

1975

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Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221

Human genetics, 1984-01, Vol.66 (2-3), p.190-192

1984

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Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region

An ovarian dysgerminoma in Down syndrome. Hypothesis about the association

De novo complex chromosomal rearrangements (CCR) involving chromosome 1, 5, and 6 resulting in microdeletion for 6q14 in a female carrier with psychotic disorder

No significant effect of monosomy for distal 21q22.3 on the down syndrome phenotype in Mirror duplications of chromosome 21

The 50th anniversary of the discovery of trisomy 21: The past, present, and future of research and treatment of Down syndrome

Eleven new cases of del(9p) and features from 80 cases

Métabolisme des substrats monocarbonés et trisomie 21: analyse de l'impact des polymorphismes génétiques

ETUDE DE LA DESCENDANCE DE SUJETS TRAITÉS PAR RADIOTHÉRAPIE PELVIENNE

Les dysmorphies liées aux aberrations chromosomiques autosomiques de l'enfant à l'adulte

Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13

Surrogate pregnancy with regard to marriage between persons of the same sex

Cystathionine beta synthase: Gene dosage effect in trisomy 21

DNA polymorphism analysis in families with recurrence of free trisomy 21

Differences in purine metabolism in patients with Down's syndrome

Failure of testicular development associated with a rearrangement of 9p24.1 proximal to the SNF2 gene

In vivo folic acid supplementation partially corrects in vitro methotrexate toxicity in patients with Down syndrome

The child and his family

An ovarian dysgerminoma in Down syndrome. Hypothesis about the association

Consequences of the effects of gene determinations

A 23-year-old woman with down syndrome, type 1 neurofibromatosis, and breast carcinoma

Excessive glutamine sensitivity in Alzheimer's disease and Down syndrome lymphocytes

Announcement of diagnosis of 21-trisomy and abandonment

Structural variation of chromosome 21 and symptoms of Down's syndrome

Analyse du caryotype dePan paniscus. Comparaison avec les autresPongidae etl'Homme

Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221

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