DeLozier-Blanchet CD - Search Results

1

Angelman syndrome due to paternal uniparental disomy of chromosome 15: a milder phenotype?

Bottani A, Robinson WP, DeLozier-Blanchet CD, Engel E, Morris MA, Schmitt B, Thun-Hohenstein L, Schinzel A. Bottani A, et al. Am J Med Genet. 1994 May 15;51(1):35-40. doi: 10.1002/ajmg.1320510109. Am J Med Genet. 1994. PMID: 8030667

2

Uniparental disomy, isodisomy, and imprinting: probable effects in man and strategies for their detection.

Engel E, DeLozier-Blanchet CD. Engel E, et al. Am J Med Genet. 1991 Sep 15;40(4):432-9. doi: 10.1002/ajmg.1320400411. Am J Med Genet. 1991. PMID: 1746607 Review.

3

Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13.

Eliez S, Morris MA, Dahoun-Hadorn S, DeLozier-Blanchet CD, Gos A, Sizonenko P, Antonarakis SE. Eliez S, et al. Am J Med Genet. 1997 Jun 13;70(3):222-8. doi: 10.1002/(sici)1096-8628(19970613)70:3<222::aid-ajmg3>3.0.co;2-y. Am J Med Genet. 1997. PMID: 9188657

4

Dysmorphology report holoprosencephaly-polydactyly syndrome: affected brother and sister with a wide spectrum of anomalies.

Delozier-Blanchet CD, Engel E. Delozier-Blanchet CD, et al. Genet Couns. 1992;3(1):57-8. Genet Couns. 1992. PMID: 1590983 No abstract available.

5

Exon skipping associated with A-->G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene.

Hutter P, Antonarakis SE, Delozier-Blanchet CD, Morris MA. Hutter P, et al. Hum Mol Genet. 1994 Apr;3(4):663-5. doi: 10.1093/hmg/3.4.663. Hum Mol Genet. 1994. PMID: 8069315 No abstract available.

6

High incidence of ectopic nucleolar organizer regions in human testicular tumors.

Neerman-Arbez M, DeLozier-Blanchet CD, Bolle JF, Rondez R, Morris M. Neerman-Arbez M, et al. Cancer Genet Cytogenet. 1993 Jan;65(1):58-63. doi: 10.1016/0165-4608(93)90059-u. Cancer Genet Cytogenet. 1993. PMID: 8381712

7

Trisomy 3 mosaicism on CVS: case report with literature review and propositions for investigation and counseling.

Delozier-Blanchet CD, Francipane L, Morris MA, Hoovers JM, Leschot NJ, Cox JN. Delozier-Blanchet CD, et al. Clin Genet. 1995 Dec;48(6):308-12. doi: 10.1111/j.1399-0004.1995.tb04115.x. Clin Genet. 1995. PMID: 8835326

8

Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping.

Bartoloni L, Blouin J, Sainsbury AJ, Gos A, Morris MA, Affara NA, DeLozier-Blanchet CD, Antonarakis SE. Bartoloni L, et al. Among authors: delozier blanchet cd. Cytogenet Cell Genet. 1999;84(3-4):188-9. doi: 10.1159/000015254. Cytogenet Cell Genet. 1999. PMID: 10393427 No abstract available.

9

[Chorionic villus sampling (CVS): level of activity and methods to resolve certain difficulties in interpretation].

Delozier-Blanchet CD, Extermann P, Morris MA, Engel E. Delozier-Blanchet CD, et al. J Genet Hum. 1989 Jan;37(1):61-9. J Genet Hum. 1989. PMID: 2715784 French.

10

Trisomy 7 in chorionic villi: follow-up studies of pregnancy, normal child, and placental clonal anomalies.

Delozier-Blanchet CD, Engel E, Extermann P, Pastori B. Delozier-Blanchet CD, et al. Prenat Diagn. 1988 May;8(4):281-6. doi: 10.1002/pd.1970080406. Prenat Diagn. 1988. PMID: 3399481

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