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Fetuin A Concentration in the Second Trimester Amniotic Fluid of Fetuses with Trisomy 21 Appears to Be Lower: Phenotypic Considerations

Mediators of Inflammation, 2012-01, Vol.2012 (2012), p.80-83

2012

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Resistin in mid-trimester amniotic fluid in trisomy 21

The journal of maternal-fetal & neonatal medicine, 2013-11, Vol.26 (16), p.1576-1580

2013

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Human embryo splitting: proof of homozygosity

Fertility and sterility, 2010, Vol.94 (4), p.S148-S148

2010

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Pregnancy following preimplantation genetic diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

Prenatal diagnosis, 2007-11, Vol.27 (11), p.1079-1083

2007

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The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis

Prenatal diagnosis, 2005-11, Vol.25 (11), p.1057-1058

2005

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Molecular analysis of transferrin receptor mRNA expression in acute myeloid leukaemia

British journal of haematology, 2001-10, Vol.115 (1), p.19-24

2001

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Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis

American journal of human genetics, 1994-03, Vol.54 (3), p.473-481

1994

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Normal phenotype with paternal uniparental isodisomy for chromosome 21

American journal of human genetics, 1993-11, Vol.53 (5), p.1074-1078

1993

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O▪44 Apoptosis and aneuploidy analysis in spermatozoa and ICSI failure

Reproductive biomedicine online, 2005, Vol.10, p.15-15

2005

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Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: Case report and review of the literature on partial trisomy 17qter

American journal of medical genetics, 1997-05, Vol.70 (1), p.87-94

1997

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The equilibria of the translational-rotational motion of two gyrostats in a Newtonian central field of forces

Astrophysics and space science, 1992-10, Vol.196 (1), p.125-142

1992

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La periodicit et la symetrie du mouvement equatorial au probl me magnetique-binaire

Celestial Mechanics, 1987-03, Vol.41 (1-4), p.371-380

1987

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Expression of recombination activating genes-1 and-2 immunoglobulin heavy chain gene rearrangements in acute myeloid leukemia: evaluation of biological and clinical significance in a series of 76 uniformly treated patients and review of the literature

Haematologica (Roma), 2003-03, Vol.88 (3), p.268

2003

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The meiotic stage of nondisjunction in trisomy 21 : determination by using DNA polymorphisms

American journal of human genetics, 1992-03, Vol.50 (3), p.544-550

1992

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Development of an Internet Security Policy for health care establishments

Medical informatics and the internet in medicine, 2000, Vol.25 (4), p.265-273

Pangalos, C. Ilioudis, G.

2000

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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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Areas of equatorial motion in the magnetic-binary problem

Celestial mechanics and dynamical astronomy, 1985-10, Vol.37 (2), p.161-170

1985

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The symplectic character of the three-dimensional magnetic-binary problem

Astrophysics and space science, 1983-10, Vol.96 (2), p.255-259

1983

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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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Partial trisomy 13 (q21.3 leads to qter) resulting from a maternal translocation t (13;21)

Annales de génétique, 1981, Vol.24 (3), p.179

1981

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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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Molecular Demonstration of BCR/ABL Fusion in a Patient with Chronic Myelogenous Leukemia with Basophilia Carrying a Variant t(16;22) (q24;q11) Philadelphia Chromosome

Hematology (Luxembourg), 1999-01, Vol.4 (3), p.211-216

1999

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Growth retardation, distinct oriental-like facies, glaucoma, brachydactyly, ventricular septal defect and speech disorder. An unknown entity

Genetic counseling, 1999, Vol.10 (3), p.245

1999

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Tay-Sachs and Sandhoff diseases: an hypothesis about the primary lesion based on hexosaminidase patterns in interspecific hybrids

Cytogenetic and genome research, 1975, Vol.14 (3-6), p.442-445

1975

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Ring-14 and trisomy 14q in the same child

Annales de génétique, 1984, Vol.27 (1), p.38

1984

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Fetuin A Concentration in the Second Trimester Amniotic Fluid of Fetuses with Trisomy 21 Appears to Be Lower: Phenotypic Considerations

Resistin in mid-trimester amniotic fluid in trisomy 21

Human embryo splitting: proof of homozygosity

Pregnancy following preimplantation genetic diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis

Molecular analysis of transferrin receptor mRNA expression in acute myeloid leukaemia

Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis

Normal phenotype with paternal uniparental isodisomy for chromosome 21

O▪44 Apoptosis and aneuploidy analysis in spermatozoa and ICSI failure

Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: Case report and review of the literature on partial trisomy 17qter

The equilibria of the translational-rotational motion of two gyrostats in a Newtonian central field of forces

La periodicit et la symetrie du mouvement equatorial au probl me magnetique-binaire

Expression of recombination activating genes-1 and-2 immunoglobulin heavy chain gene rearrangements in acute myeloid leukemia: evaluation of biological and clinical significance in a series of 76 uniformly treated patients and review of the literature

The meiotic stage of nondisjunction in trisomy 21 : determination by using DNA polymorphisms

Development of an Internet Security Policy for health care establishments

Pure partial trisomy of the short arm of chromosome 5

Areas of equatorial motion in the magnetic-binary problem

The symplectic character of the three-dimensional magnetic-binary problem

DNA polymorphism analysis in families with recurrence of free trisomy 21

Partial trisomy 13 (q21.3 leads to qter) resulting from a maternal translocation t (13;21)

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

Molecular Demonstration of BCR/ABL Fusion in a Patient with Chronic Myelogenous Leukemia with Basophilia Carrying a Variant t(16;22) (q24;q11) Philadelphia Chromosome

Growth retardation, distinct oriental-like facies, glaucoma, brachydactyly, ventricular septal defect and speech disorder. An unknown entity

Tay-Sachs and Sandhoff diseases: an hypothesis about the primary lesion based on hexosaminidase patterns in interspecific hybrids

Ring-14 and trisomy 14q in the same child

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