J. Mattéi

发表

Physicians' acceptability of termination of pregnancy after prenatal diagnosis in southern france

S. Aymé, J. Gouvernet, C. Julian, 1989, Prenatal diagnosis.

Erythrocyte copper levels in children with trisomy 21.

M. Mattei, S. Aymé, B. Mallet, 2008, Journal of mental deficiency research.

Wilms' tumor, malformative syndrome, mental retardation and de novo constitutional translocation, t(7;13)(q36;q13)

C. Raybaud, J. Bernard, J. Mattéi, 2004, European Journal of Pediatrics.

Study of a family with a fragile site of the X chromosome at Xq27–28 without mental retardation

F. Birg, N. Philip, M. Mattei, 1989, Human Genetics.

Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.

G. Lathrop, R. Heilig, P. Jacobs, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Prenatal detection of a 17p11.2 duplication resulting from a rare recombination event and novel PCR-based strategy for molecular identification of Charcot-Marie-Tooth disease type 1A

N. Philip, N. Lévy, S. Tardieu, 2000, European Journal of Human Genetics.

Immunoreactive Cu SOD and Mn SOD in the circulating blood cells from normal and trisomy 21 subjects.

J. Mattéi, F. Giraud, A. Baret, 1981, Biochemical and biophysical research communications.

Mapping of the human retinoic acid receptor to the q21 band of chromosome 17

P. Chambon, M. Mattei, M. Petkovich, 1988, Human Genetics.

X-Autosome translocations: Cytogenetic characteristics and their consequences

M. Mattei, S. Aymé, J. Mattéi, 2004, Human Genetics.

CpG dinucleotides are mutation hot spots in phenylketonuria.

A. Munnich, S. Lyonnet, C. Caillaud, 1989, Genomics.

Phenotype–genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients

P. Auquier, N. Philip, M. Mattei, 1999, European Journal of Human Genetics.

[Angelman syndrome].

M. Mattei, A. Moncla, P. Malzac, 1994, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Prader-Willi syndrome: Diagnostic strategy with a cytogenetic and molecular approach

M. Mattéi, A. Moncla, P. Malzac, 1993, Neuromuscular Disorders.

Syndrome of polydactyly, cleft lip, lingual hamartomas, renal hypoplasia, hearing loss, and psychomotor retardation: variant of the Mohr syndrome or a new syndrome?

J. Mattéi, S. Aymé, 1983, Journal of medical genetics.

Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation

F. Birg, N. Philip, M. Mattei, 1988, Human Genetics.

Genetic aspects of artificial insemination by donor (AID). Indications, surveillance and results

J. Mattéi, B. Marec, F. Cecos, 1983, Clinical genetics.

XNP mutation in a large family with Juberg-Marsidi syndrome

A. Munnich, S. Lyonnet, L. Villard, 1996, Nature Genetics.

Physical mapping of an Xq-proximal interstitial duplication in a male

N. Philip, M. Mattei, A. Moncla, 1992, Human Genetics.

Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndrome

M. Mattei, A. Moncla, M. Fontès, 1993, Human Genetics.

Assignment of the gene for neuroendocrine protein 7B2 (SGNE1 locus) to mouse chromosome region 2[E3-F3] and to human chromosome region 15q11-q15.

N. Seidah, M. Chrétien, M. Mattei, 1990, Genomics.

Singularities of Codimension One Complex Foliations a Partial Survey

J. Mattéi, D. Cerveau, 1985 .

A First Molecular Approach Towards CGG Repeat Expansion in FMR1 Gene in Systemic Lupus Erythematosus and in Sjögren’s Syndrome: A Preliminary Report

J. Serratrice, P. Disdier, P. Weiller, 2000, Clinical Rheumatology.

Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14–q21

M. Mattei, J. Cartron, Y. Colin, 1986, Human Genetics.

Chromosomal localization of the three members of the jun proto-oncogene family in mouse and man.

J. Guénet, M. Yaniv, M. Mattei, 1990, Oncogene.

Constitutional chromosomal breakage

M. Mattei, S. Aymé, J. Mattéi, 1976, Human Genetics.

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site

K. Davies, R. Heilig, J. Mandel, 2004, Human Genetics.

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome

N. Philip, J. Mandel, M. Mattei, 2004, Human Genetics.

Four new cases of dicentric Y chromosomes

M. Mattei, J. Mattéi, F. Giraud, 1977, Human Genetics.

Y autosome translocation and complex chromosome rearrangement in cri du chat syndrome.

M. Mattei, J. Mattéi, F. Giraud, 1978, Journal of medical genetics.

HLA and trisomy 21. Confirmation of a trend of restricted HLA heterogeneity in parents of Down syndrome children.

J. Mattéi, P. Mercier, S. Aymé, 1984, American journal of human genetics.

Immunoreactive Copper‐Zinc Superoxide‐dismutase (SOD‐1) in Mosaic Trisomy 21 and Normal Subjects

M. Mattei, J. Mattéi, A. Baret, 1984, Acta paediatrica Scandinavica.

Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects

M. Mattei, J. Mattéi, Y. Aurran, 1976, Human Genetics.

Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis

M. Mattei, J. Mattéi, N. Souiah, 2004, Human Genetics.

[Partial trisomy 13 due to maternal translocation t(2;13)].

M. Mattei, J. Mattéi, F. Giraud, 1977, Annales de genetique.

X-linked mental retardation with the fragile X. A study of 15 families

M. Mattei, M. Auger, J. Mattéi, 2004, Human Genetics.

Expression in lymphocyte and fibroblast culture of the fragile X chromosome: A new technical approach

M. Mattei, J. Mattéi, F. Giraud, 2004, Human Genetics.

The Use of Prenatal Diagnosis for Psychiatric Diseases

J. Mattéi, 1991 .

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.

A. Aurias, J. Delabar, Z. Rahmani, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Achondroplasia in sibs of normal parents.

N. Philip, M. Auger, J. Mattéi, 1988, Journal of medical genetics.

Localization of human platelet proteoglycan gene to chromosome 10, band q22.1, by in situ hybridization

M. Mattei, P. Jollès, P. Alliel, 1989, Human Genetics.

Immunoreactive Cu-SOD and Mn-SOD in lymphocytes sub-populations from normal and trisomy 21 subjects according to age.

J. Mattéi, A. Baret, P. Rebuffel, 1983, Life sciences.

Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile site.

M. Mattei, J. Rey, B. Jordan, 1988, American journal of medical genetics.

Large scale physical mapping in the q27 region of the human X chromosome: the coagulation factor IX gene and the mcf.2 transforming sequence are separated by at most 270 kilobase pairs and are surrounded by several ‘HTF islands’.

D. Birnbaum, P. Pontarotti, G. Chimini, 1987, The EMBO journal.

Coffin-Lowry syndrome in sibs.

R. Laframboise, J. Mattéi, F. Rouault, 1981, American journal of medical genetics.

Distribution of spontaneous chromosome breaks in man.

M. Mattei, S. Aymé, J. Mattéi, 1979, Cytogenetics and cell genetics.

Localization of the human NCAM gene to band q23 of chromosome 11: the third gene coding for a cell interaction molecule mapped to the distal portion of the long arm of chromosome 11

M. Mattei, C. Goridis, B. Jordan, 1986, The Journal of cell biology.

Assignment of the mouse desmin gene to chromosome 1 band C3.

M. Mattei, D. Paulin, J. Mattéi, 1990, Genetical research.

GENTIC: a computerized medical genetic case record system.

J Gouvernet, S Aymé, Y Aurran, 1982, American journal of medical genetics.

Prenatal diagnosis of Fryns' syndrome

N. Philip, S. Aymé, J. Mattéi, 1992, Prenatal diagnosis.

Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases.

M. Mattei, A. Moncla, M. Auger, 1991, Journal of medical genetics.

Quantitative and qualitative study of acrocentric associations in 109 normal subjects

M. Mattei, J. Gouvernet, J. Mattéi, 1976, Human Genetics.

The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome

D. Pham‐Dinh, M. Mattei, P. Jollès, 1986, Human Genetics.

In situ hybridization and pulsed-field gel analysis define two major minisatellite loci: 1q23 for minisatellite 33.6 and 7q35-q36 for minisatellite 33.15.

M. Mattei, G. Chimini, B. Jordan, 1989, Genomics.

Morquio syndrome: Clinical findings in 11 patients with MPS IVA and 2 patients with MPS IVB

W. Holzgreve, K. Figura, H. Kresse, 2004, Human Genetics.

Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation

M. Mattei, J. Mattéi, R. Bernard, 1979, Human Genetics.

Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counselling

P Malzac, J F Mattei, N. Philip, 1999, Journal of medical genetics.

[4p monosomy with paternal t(13;14) (p11;p11) translocation].

J. Lambert, N. Ayraud, J. Mattéi, 1979, Pediatrie.

Transmission of mental retardation with fragile X site by two normal transmitter brothers.

M. Mattei, C. Piquet, J. Mattéi, 1991, American journal of medical genetics.

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

M. Jaye, G. Camerino, J. Mandel, 1983, Nature.

Structural anomalies of the X chromosome and inactivation center

M. Mattei, J. Mattéi, F. Giraud, 1981, Human Genetics.

A dynamic study in two new cases of X chromosome translocations

M. Mattei, J. Mattéi, F. Giraud, 1978, Human Genetics.

Assignment of the humanhap retinoic acid receptor RARβ gene to the p24 band of chromosome 3

A. Dejean, M. Mattei, A. Marchio, 1988, Human Genetics.

Assignment of the human progesterone receptor to the q22 band of chromosome 11

P. Chambon, A. Krust, M. Mattei, 2004, Human Genetics.

The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice

D. Simon, P. Avner, D. Pham‐Dinh, 1986, Nature.

Monosomy 21: a new case confirmed by in situ hybridization

N. Philip, M. Mattei, J. Mattéi, 1987, Human Genetics.

Three new cases of partial monosomy 21 resulting from one ring 21 chromosome and two unbalanced reciprocal translocations

N. Philip, M. Mattei, J. Mattéi, 1984, European Journal of Pediatrics.

Down syndrome critical region around D21S55 on proximal 21q22.3.

A. Aurias, Z. Rahmani, Z. Chettouh, 2005, American journal of medical genetics. Supplement.

Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21.

J. Fermanian, Z. Rahmani, Z. Chettouh, 1990, American journal of human genetics.

Trisomy 21 for the region 21q223: Identification by high-resolution R-banding patterns

M. Mattei, J. Mattéi, M. A. Baeteman, 1981, Human Genetics.

Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter syndrome.

N. Philip, I. Boccaccio, C. Piquet, 1991, American journal of medical genetics.

Peripheral and central 5-hydroxytryptamine in trisomy 21.

J. Mattéi, J. Ternaux, J. Ardissone, 1979, Life sciences.

Chromosomal localization of the mouse gene coding for vimentin.

M. Mattei, D. Paulin, J. Mattéi, 1989, Genetical research.

Immunoreactive SOD‐1 in Amniotic Fluid, Amniotic Cells and Fibroblasts from Trisomy 21 Fetus

M. Gamerre, M. Mattei, J. Mattéi, 1985, Acta paediatrica Scandinavica.

[Acrocentric associations in parents of mongol children].

M. Mattei, S. Aymé, J. Mattéi, 1974, Humangenetik.

Dicentric Robertsonian translocations in man

M. Mattei, S. Aymé, J. Mattéi, 2004, Human Genetics.

Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents

M. Mattei, J. Mattéi, F. Giraud, 1979, Human Genetics.

Advantages of silver staining in seven rearrangements of acrocentric chromosomes, excluding robertsonian translocations

M. Mattei, J. Mattéi, F. Giraud, 2004, Human Genetics.

A girl with mosaicism for a dicentric X chromosome (45,X/46,X,dic(X) (Xqter→p22::p22→qter))

M. Mattei, J. Mattéi, F. Giraud, 1977, Human Genetics.

[Trisomy 8 in mosaicism].

M. Mattei, J. Mattéi, R. Bernard, 1975, Archives francaises de pediatrie.

Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8p

M. Mattei, J. Mattéi, J. Ardissone, 1980, Human Genetics.

Chromosome Studies in 1942 Women before Artificial Insemination with Donor Semen

M. Mattei, M. Guichaoua, J. Mattéi, 1980 .

Unexpected Inheritance of the (CGG)n Trinucleotide Expansion in a Fragile X Syndrome Family

V. Biancalana, A. Moncla, I. Boccaccio, 1996, European journal of human genetics : EJHG.

Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7 *

N. Philip, M. Mattei, J. Mattéi, 1985, Clinical genetics.

Trisomy 21q223 and Down's phenotype correlation evidenced by in situ hybridization

N. Philip, M. Mattei, J. Mattéi, 1988, Human Genetics.

Prader-Willi syndrome and chromosome 15

M. Mattei, J. Mattéi, F. Giraud, 1983, Human Genetics.

Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase B

M. Mattei, J. Mattéi, P. Balestrazzi, 2004, Human Genetics.

Pericentric inversion, inv(9) (p22 q32), in the father of a child with a duplication‐deletion of chromosome 9 and gene dosage effect for adenylate kinase‐1

M. Mattei, J. Mattéi, J. Ardissone, 1980, Clinical genetics.

Assignment of human uroporphyrinogen decarboxylase (URO-D) to the p34 band of chromosome 1

M. Mattei, P. Romeo, D. Beaupain, 1986, Human Genetics.

Blepharophimosis-mental retardation syndrome and terminal deletion of chromosome 3p.

N. Philip, A. Moncla, J. Mattéi, 1995, Journal of medical genetics.

Thalassaemia in Azerbaijan A recent study referred to the incidence of molecular mutations and the clinical picture of thalassaemia in Azerbaijan

J. Mattéi, 2022 .

Mapping class group of a plane curve germ

D. Marín, J. Mattéi, 2011 .

Mapping Class Group d'un germe de courbe plane singuli\`ere

J. Mattéi, D. Mar'in, 2010, 1004.2837.

Recent acquisitions of the Library and Research Service, ICRC

J. Mattéi, Gérard A. Henry Dunant, 2010, International Review of the Red Cross.

Faciliter l’adoption nationale

J. Hureau, M. Adolphe, J. L. Gall, 2011 .

Nicomachus of Gerasa and the Arithmetic Scale of the Divine

J. Mattéi, 2005 .

The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21).

A. Munnich, S. Lyonnet, A. Moncla, 1993, American journal of human genetics.

Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.

S. Thibodeau, K. Davies, S. Kenwrick, 1987, Nucleic acids research.

Duchenne type muscular dystrophy and consanguinity: difficulties in pedigree analysis.

J. Garnier, J. Mattéi, J. Pelissier, 1979, Journal of medical genetics.

Origin of the extra chromosome in trisomy 21

M. Mattei, S. Aymé, J. Mattéi, 1979, Human Genetics.

Chromosomal localization of the mouse gene coding for the 68 kDa neurofilament subunit

D. Paulin, J. Mattéi, P. Duprey, 1989, Biology of the cell.

[Somatic future of children with kwashiorkor].

J. Mattéi, P. Satgé, V. Dan, 1970, Annales de pediatrie.

Subacute myelocytic leukemia associated with the philadelphia chromosome and supplementary translocation : 9-12.

M. Mattei, J. Mattéi, F. Giraud, 1977, Biomedicine / [publiee pour l'A.A.I.C.I.G.].

POLYMORPHIC DNA MARKERS IN PRENATAL DIAGNOSIS OF FRAGILE X SYNDROME

J. Mandel, M. Mattei, J. Boué, 1985, The Lancet.

Genetic Analysis of the Fragile X-Mental Retardation Syndrome with Polymorphic DNA Markers

M. Mattéi, G. Camerino, B. Arveiler, 1986 .

[Fertility of 45,X-46,XX and 45,X-46,XX-47,XXX women].

A. Stahl, J. Mattéi, R. Bernard, 1970, Annales de genetique.

Monodromy and topological classification of germs of holomorphic foliations

J. Mattéi, D. Mar'in, 2010, 1004.1552.

Topological Moduli Space for Germs of Holomorphic Foliations

J. Mattéi, D. Mar'in, 'Eliane Salem, 2017, International Mathematics Research Notices.

Topology of singular holomorphic foliations along a compact divisor

J. Mattéi, D. Mar'in, 2012, 1206.2121.

Modules formels locaux de feuilletages holomorphes

J. Mattéi, É. Salem, 2004, math/0402256.

COMPLETE SYSTEMS OF TOPOLOGICAL AND ANALYTICAL INVARIANTS FOR A GENERIC FOLIATION OF (C, 0)

J. Mattéi, É. Salem, 2004 .

Complete systems of topological and analytical invariants for a generic foliation of $( {\Bbb C}^2, 0 )$

J. Mattéi, É. Salem, 1997 .

Parental origin of del(15)(q11-q13) in Angelman and Prader-Willi syndromes.

R. Zori, A. Moncla, J. Mattéi, 1990, American journal of medical genetics.

Maternal age and origin of non-disjunction in trisomy 21.

M. Mattei, S. Aymé, J. Mattéi, 1980, Journal of medical genetics.

[Balanced chromosome rearrangements with abnormal phenotype].

N. Philip, M. Mattei, J. Mattéi, 1988, Journal de genetique humaine.

Molecular analysis of an isoYq Chromosome in a sterile male mouse

M. Mitchell, N. Lévy, P. Boer, 1996, Mammalian Genome.

The acrocallosal syndrome

N. Philip, J. Mattéi, F. Giraud, 1988, European Journal of Pediatrics.

Le syndrome d'Angelman

M. Mattei, A. Moncla, P. Malzac, 1994 .

Bilateral retinoblastoma with de novo constitutional balanced translocation t(2;9)(q11;q11)

M. Mattei, J. Mattéi, P. Balestrazzi, 1984, European Journal of Pediatrics.

[Interstitial deletion of chromosome 7 (7q33 to q35)].

M. Mattei, J. Mattéi, P. Rebuffel, 1982, Journal de genetique humaine.

Assignment of the human hap retinoic acid receptor RAR beta gene to the p24 band of chromosome 3.

A. Dejean, M. Mattei, A. Marchio, 1988, Human genetics.

The gene encoding the large human neurofilament subunit (NF-H) maps to the q121–q131 region on human chromosome 22

D. Pham‐Dinh, M. Mattei, J. Mattéi, 1988, Human Genetics.

Vector fields in the vicinity of a circle of critical points

M. Teixeira, J. Mattéi, 1986 .

Partial inversion of the secondary constriction of chromosome 9. Does it exist?

M. Mattei, M. Guichaoua, J. Mattéi, 2004, Human Genetics.