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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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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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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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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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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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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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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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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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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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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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Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases

Annales de génétique, 2004-07, Vol.47 (3), p.315-324

2004

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Homocysteine and the methotrexate toxicity in trisomy 21

Cancer chemotherapy and pharmacology, 1991-01, Vol.27 (4), p.331-332

1991

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Regional mapping of liver type 6 phosphofructokinase isoenzyme on chromosome 21

Human genetics, 1984-01, Vol.68 (2), p.136-137

1984

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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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No association between common polymorphisms in genes of folate and homocysteine metabolism and the risk of Down's syndrome among French mothers

British journal of nutrition, 2005-08, Vol.94 (2), p.166-169

2005

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Pure partial trisomy of the short arm of chromosome 5

Human genetics, 1989-06, Vol.82 (3), p.296-298

1989

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Segregation of three reciprocal translocations in the same family: t(3;4), t(5;10), and t(15;21)

American journal of medical genetics, 1992-03, Vol.42 (5), p.716-719

1992

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Inverted neurons in agyria: a Golgi study of a case with abnormal chromosome 17

Human genetics, 1986-08, Vol.73 (4), p.374-378

1986

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Homocysteine concentrations in adults with trisomy 21: effect of B vitamins and genetic polymorphisms

The American journal of clinical nutrition, 2004-12, Vol.80 (6), p.1551-1557

2004

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Reflection analysis: a new optical method. Evidence of mitotic inter-chromosomal RNA

Cytogenetics and cell genetics, 1986, Vol.41 (1), p.54

1986

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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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Contribution of magnetic resonance imaging to the knowledge of CNS malformations related to chromosomal aberrations

Human genetics, 1987-07, Vol.76 (3), p.265-273

1987

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ETUDE DE LA DESCENDANCE DE SUJETS TRAITÉS PAR RADIOTHÉRAPIE PELVIENNE

Human heredity, 2004-07, Vol.6 (2), p.204-216

2004

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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

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

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

Differences in purine metabolism in patients with Down's syndrome

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

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

Cystathionine beta synthase: Gene dosage effect in trisomy 21

DNA polymorphism analysis in families with recurrence of free trisomy 21

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

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

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

Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases

Homocysteine and the methotrexate toxicity in trisomy 21

Regional mapping of liver type 6 phosphofructokinase isoenzyme on chromosome 21

Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221

No association between common polymorphisms in genes of folate and homocysteine metabolism and the risk of Down's syndrome among French mothers

Pure partial trisomy of the short arm of chromosome 5

Segregation of three reciprocal translocations in the same family: t(3;4), t(5;10), and t(15;21)

Inverted neurons in agyria: a Golgi study of a case with abnormal chromosome 17

Homocysteine concentrations in adults with trisomy 21: effect of B vitamins and genetic polymorphisms

Reflection analysis: a new optical method. Evidence of mitotic inter-chromosomal RNA

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

Contribution of magnetic resonance imaging to the knowledge of CNS malformations related to chromosomal aberrations

ETUDE DE LA DESCENDANCE DE SUJETS TRAITÉS PAR RADIOTHÉRAPIE PELVIENNE

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