Delezoide AL - Search Results

1

Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain.

Abitbol M, Menini C, Delezoide AL, Rhyner T, Vekemans M, Mallet J. Abitbol M, et al. Among authors: delezoide al. Nat Genet. 1993 Jun;4(2):147-53. doi: 10.1038/ng0693-147. Nat Genet. 1993. PMID: 8348153

2

Insulin-like 4 (INSL4) gene expression in human embryonic and trophoblastic tissues.

Laurent A, Rouillac C, Delezoide AL, Giovangrandi Y, Vekemans M, Bellet D, Abitbol M, Vidaud M. Laurent A, et al. Among authors: delezoide al. Mol Reprod Dev. 1998 Oct;51(2):123-9. doi: 10.1002/(SICI)1098-2795(199810)51:2<123::AID-MRD1>3.0.CO;2-S. Mol Reprod Dev. 1998. PMID: 9740319

3

Expression of the RET proto-oncogene in human embryos.

Attié-Bitach T, Abitbol M, Gérard M, Delezoide AL, Augé J, Pelet A, Amiel J, Pachnis V, Munnich A, Lyonnet S, Vekemans M. Attié-Bitach T, et al. Among authors: delezoide al. Am J Med Genet. 1998 Dec 28;80(5):481-6. doi: 10.1002/(sici)1096-8628(19981228)80:5<481::aid-ajmg8>3.0.co;2-6. Am J Med Genet. 1998. PMID: 9880212

4

PAX-genes expression during human embryonic development, a preliminary report.

Gérard M, Abitbol M, Delezoide AL, Dufier JL, Mallet J, Vekemans M. Gérard M, et al. Among authors: delezoide al. C R Acad Sci III. 1995 Jan;318(1):57-66. C R Acad Sci III. 1995. PMID: 7757805

5

Expression of the PAX2 gene in human embryos and exclusion in the CHARGE syndrome.

Tellier AL, Amiel J, Delezoide AL, Audollent S, Augé J, Esnault D, Encha-Razavi F, Munnich A, Lyonnet S, Vekemans M, Attié-Bitach T. Tellier AL, et al. Among authors: delezoide al. Am J Med Genet. 2000 Jul 17;93(2):85-8. doi: 10.1002/1096-8628(20000717)93:2<85::aid-ajmg1>3.0.co;2-b. Am J Med Genet. 2000. PMID: 10869107

6

Abnormal FGFR 3 expression in cartilage of thanatophoric dysplasia fetuses.

Delezoide AL, Lasselin-Benoist C, Legeai-Mallet L, Brice P, Senée V, Yayon A, Munnich A, Vekemans M, Bonaventure J. Delezoide AL, et al. Hum Mol Genet. 1997 Oct;6(11):1899-906. doi: 10.1093/hmg/6.11.1899. Hum Mol Genet. 1997. PMID: 9302269

7

Regional and cellular specificity of the expression of TPRD, the tetratricopeptide Down syndrome gene, during human embryonic development.

Rachidi M, Lopes C, Gassanova S, Sinet PM, Vekemans M, Attie T, Delezoide AL, Delabar JM. Rachidi M, et al. Among authors: delezoide al. Mech Dev. 2000 May;93(1-2):189-93. doi: 10.1016/s0925-4773(00)00259-8. Mech Dev. 2000. PMID: 10781955 Free article.

8

Waardenburg syndrome in man and splotch mutants in the mouse: a paradigm of the usefulness of linkage and synteny homologies in mouse and man for the genetic analysis of human congenital malformations.

Delezoide AL, Vekemans M. Delezoide AL, et al. Biomed Pharmacother. 1994;48(8-9):335-9. doi: 10.1016/0753-3322(94)90047-7. Biomed Pharmacother. 1994. PMID: 7858167 Review.

9

Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qter.

Morichon-Delvallez N, Delezoide AL, Vekemans M. Morichon-Delvallez N, et al. Among authors: delezoide al. J Med Genet. 1993 Jun;30(6):521-4. doi: 10.1136/jmg.30.6.521. J Med Genet. 1993. PMID: 8326499 Free PMC article. Review.

10

A new lethal syndrome of exomphalos, short limbs, and macrogonadism.

Faivre L, Delezoide AL, Narcy F, Razavi F, Bouvier R, Cormier-Daire V, Briard ML, Lyonnet S, Vekemans M, Munnich A, Le Merrer M. Faivre L, et al. Among authors: delezoide al. J Med Genet. 1999 Feb;36(2):131-6. J Med Genet. 1999. PMID: 10051012 Free PMC article.

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