J. Taillemite

发表

Severe hypophosphatasia: Characterization of fifteen novel mutations in the ALPL gene

S. Mansour, S. Holder, A. Norman, 2003, Human mutation.

Pierre Robin sequence and interstitial deletion 2q32.3-q33.2.

C. Houdayer, M. Vazquez, F. Vialard, 2001, American journal of medical genetics.

Two new cases of papillary renal cell carcinoma with t(X;1)(p11;q21) in females.

G. Leverger, L. Boccon-Gibod, J. Couturier, 1999, Cancer genetics and cytogenetics.

Paternal age and Down's syndrome diagnosed prenatally: No association in French data

C. Stoll, M. Roth, A. Boué, 1983, Prenatal diagnosis.

Different proximal and distal rearrangements of chromosome 7q associated with holoprosencephaly.

M. Gonzalès, F. Encha-Razavi, L. Carbillon, 1997, Journal of medical genetics.

Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid cases

J. Soulier, C. Bastard, S. Taviaux, 2003, Genes, chromosomes & cancer.

Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q

M. Portnoï, B. Crickx, F. Bouscarat, 1999, Journal of medical genetics.

Multiple chromosome abnormalities in patients with acute leukemia after autologous bone marrow transplantation using total body irradiation and marrow purged with mafosfamide.

L. Douay, A. Najman, M. Lopez, 1993, Leukemia.

22q11.2 duplication syndrome: Two new familial cases with some overlapping features with DiGeorge/velocardiofacial syndromes

M. Portnoï, N. Gruchy, V. Malan, 2005, American journal of medical genetics. Part A.

A variant translocation (9;22;22) with local extramedullary monoblastic transformation in CML.

M. Portnoï, N. Abdelmoula, J. Taillemite, 2000, Cancer genetics and cytogenetics.

CHROMOSOME ABNORMALITIES AFTER AUTOLOGOUS BONE MARROW TRANSPLANTATION WITH MARROW TREATED BY CYCLOPHOSPHAMIDE DERIVATIVES

L. Douay, A. Najman, M. Lopez, 1985, The Lancet.

Karyotypes of 1142 Couples With Recurrent Abortion

M. Portnoï, J. Taillemite, N. Joyē, 1988, Obstetrics and gynecology.

A case of ring Y chromosome

J. Taillemite, J. V. Akker, J. Bouillie, 1978, Human Genetics.

Semen analysis in subfertile balanced-translocation carriers.

N. Joye, J. Taillemite, J. van den Akker, 1980, Fertility and sterility.

[Partial trisomy 10q dueto familial translocation t(10q-; 22p-plus)].

J. Taillemite, C. Roux, G. Baheux-Morlier, 1974, Annales de genetique.

Functional disomy of Xp including duplication of DAX1 gene with sex reversal due to t(X;Y)(p21.2;p11.3)

B. Devauchelle, F. Vialard, M. Portnoï, 2004, American journal of medical genetics. Part A.

Whole-arm translocations between chromosome 1 and acrocentric G chromosomes are associated with a poor prognosis for spermatogenesis: two new cases and review of the literature.

F. Vialard, M. Portnoï, J. Selva, 2006, Fertility and sterility.

Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families

J. Boué, A. Boué, J. Taillemite, 1975, Humangenetik.

Prenatal diagnosis by FISH of a 22q11 deletion in two families.

M. Gonzalès, M. Portnoï, J. Taillemite, 1998, Journal of medical genetics.

Meiotic behaviour of familial pericentric inversions of chromosomes 1 and 9.

Y. Rumpler, M. Guichaoua, J. Luciani, 1986, Annales de genetique.

[A new case of ring chromosome 9].

N. Joye, J. Taillemite, J. van den Akker, 1983, La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris.

[Fetal karyotyping of fetal blood obtained from the umbilical vein using ultrasound].

F. Daffos, M. Capella-Pavlovsky, F. Forestier, 1985, Journal de gynecologie, obstetrique et biologie de la reproduction.

Diaphanospondylodysostosis (DSD): Confirmation of a recessive disorder with abnormal vertebral ossification and nephroblastomatosis

A. Verloes, M. Gonzalès, F. Encha-Razavi, 2005, American journal of medical genetics. Part A.

Paternal age and Down's syndrome diagnosed prenatally: No association in French data

C. Stoll, M. Roth, A. Boué, 1983 .

Usefulness of Fluorescence in situ Hybridization for the Diagnosis of Turner Mosaic Fetuses with Small Ring X Chromosomes

M. Gonzalès, N. Berkane, J. Siffroi, 2000, Fetal Diagnosis and Therapy.

Loop formation and synaptic adjustment in a human male heterozygous for two pericentric inversions

M. Guichaoua, J. Luciani, M. Morazzani, 2004, Chromosoma.

A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata.

C. Petit, D. Weil, B. Boudailliez, 1993, Human molecular genetics.

[Interstitial deletion of the long arm of one 11 chromosome].

J. Taillemite, C. Roux, B. G. Morlier, 1975, Annales de Genetique.

[Ring chromosome 10: 46,XX,r(10)(p15q26)].

S. Despoisse, J. Taillemite, A. Broustet, 1982, Annales de genetique.

[Possible localization of the glutathione reductase (EC 1.6.4.2) on the 8p21 band].

J. Lejeune, M. Rethoré, J. Couturier, 1977, Annales de genetique.

[Partial trisonomy 22].

J. Taillemite, J. van den Akker, N. Leporrier, 1977, Annales de genetique.

[Adenomegalic forms of chronic myeloid leukemia].

N. Gorin, A. Najman, J. Taillemite, 1975, Annales de medecine interne.

[Teratogenic action by rubidomycin in the rat].

J. Taillemite, C. Roux, 1969, Comptes rendus des seances de la Societe de biologie et de ses filiales.

Deregulation of hexose transporter expression in Caco-2 cells by ras and polyoma middle T oncogenes.

A. Cadoret, J. Capeau, G. Cherqui, 1996, The American journal of physiology.

Immortalization and neoplastic transformation of fetal rat intestinal epithelial cells: morphological and cytogenetic analysis, (proto)oncogene expression and effect of gamma-interferon on cell growth.

S. Ito, V. Barbu, C. Gespach, 1990, Digestion.

Chromosomal breakage and teratogenesis.

I. Emerit, J. Taillemite, C. Roux, 1971, Teratology.

[Crying cat disease associated with complex chromosome rearrangement in a dizygotic twin].

J. Taillemite, L. Cathelineau, C. Roux, 1973, Annales de Genetique.