Petit P - Search Results

1

Multiple small accessory marker chromosomes from different centromeric origin in a moderately mentally retarded male.

Vermeesch JR, Duhamel H, Petit P, Falzetti D, Fryns JP, Marynen P. Vermeesch JR, et al. Among authors: petit p. Hum Genet. 1999 Dec;105(6):611-8. doi: 10.1007/s004399900184. Hum Genet. 1999. PMID: 10647897

2

Normal/trisomy 13 mosaicism in a 38-year-old male.

Petit P, Fryns JP. Petit P, et al. Genet Couns. 1994;5(3):311-4. Genet Couns. 1994. PMID: 7811434

3

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.

Devriendt K, Petit P, Matthijs G, Vermeesch JR, Holvoet M, De Muelenaere A, Marynen P, Cassiman JJ, Fryns JP. Devriendt K, et al. Among authors: petit p. J Med Genet. 1997 May;34(5):395-9. doi: 10.1136/jmg.34.5.395. J Med Genet. 1997. PMID: 9152837 Free PMC article.

4

Interstitial telomeric sequences at the junction site of a jumping translocation.

Vermeesch JR, Petit P, Speleman F, Devriendt K, Fryns JP, Marynen P. Vermeesch JR, et al. Among authors: petit p. Hum Genet. 1997 Jun;99(6):735-7. doi: 10.1007/s004390050440. Hum Genet. 1997. PMID: 9187665

5

Interstitial deletion 2p accompanied by marker chromosome formation of the deleted segment resulting in a stable acentric marker chromosome.

Petit P, Fryns JP. Petit P, et al. Genet Couns. 1997;8(4):341-3. Genet Couns. 1997. PMID: 9457505

6

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).

Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP. Petit P, et al. Genet Couns. 1998;9(3):215-21. Genet Couns. 1998. PMID: 9777345

7

Acrofacial dysostosis syndrome type Rodriguez: a new lethal MCA syndrome.

Petit P, Moerman P, Fryns JP. Petit P, et al. Am J Med Genet. 1992 Feb 1;42(3):343-5. doi: 10.1002/ajmg.1320420318. Am J Med Genet. 1992. PMID: 1536176

8

Full 69,XXY triploidy and sex-reversal: a further example of true hermaphrodism associated with multiple malformations.

Petit P, Moerman P, Fryns JP. Petit P, et al. Clin Genet. 1992 Apr;41(4):175-7. doi: 10.1111/j.1399-0004.1992.tb03658.x. Clin Genet. 1992. PMID: 1576753

9

Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effect.

Petit P, Fryns JP. Petit P, et al. Genet Couns. 1990;1(2):179-84. Genet Couns. 1990. PMID: 2081002

10

The various phenotypes in Xp deletion. observations in eleven patients.

Fryns JP, Petit P, Van den Berghe H. Fryns JP, et al. Among authors: petit p. Hum Genet. 1981;57(4):385-7. doi: 10.1007/BF00281690. Hum Genet. 1981. PMID: 7286978 No abstract available.

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