Delobel B - Search Results

1

Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.

Chettouh Z, Croquette MF, Delobel B, Gilgenkrants S, Leonard C, Maunoury C, Prieur M, Rethoré MO, Sinet PM, Chery M, et al. Chettouh Z, et al. Among authors: delobel b. Am J Hum Genet. 1995 Jul;57(1):62-71. Am J Hum Genet. 1995. PMID: 7611297 Free PMC article.

2

Molecular mapping of a Yq deletion in a patient with normal stature.

Rousseaux-Prévost R, Rigot JM, Delobel B, Lesur P, Collier F, Croquette MF, Gauthier A, Mazeman E, Rousseaux J. Rousseaux-Prévost R, et al. Among authors: delobel b. Hum Genet. 1996 Oct;98(4):505-7. doi: 10.1007/s004390050248. Hum Genet. 1996. PMID: 8792831

3

Synaptic behaviour of sex chromosome in two XYY men.

Gabriel-Robez O, Delobel B, Croquette MF, Rigot JM, Djlelati R, Rumpler Y. Gabriel-Robez O, et al. Among authors: delobel b. Ann Genet. 1996;39(3):129-32. Ann Genet. 1996. PMID: 8839884

4

[Fragile X syndrome is still unrecognized: efficacy of molecular diagnosis in mentally retarded probands].

Cossée M, Moutou C, Biancalana V, Bouix JC, Plessis G, Delobel B, Croquette MF, Gilgenkrantz S, Lambert JC, Malpuech G, Stoll C, Lanoe JL, Pechevis M, Mandel JL. Cossée M, et al. Among authors: delobel b. Arch Pediatr. 1997 Mar;4(3):227-36. doi: 10.1016/s0929-693x(97)87235-1. Arch Pediatr. 1997. PMID: 9181015 French.

5

Y-autosome translocation and infertility: usefulness of molecular, cytogenetic and meiotic studies.

Delobel B, Djlelati R, Gabriel-Robez O, Croquette MF, Rousseaux-Prevost R, Rousseaux J, Rigot JM, Rumpler Y. Delobel B, et al. Hum Genet. 1998 Jan;102(1):98-102. doi: 10.1007/s004390050660. Hum Genet. 1998. PMID: 9490306

6

[Smith-Magenis syndrome].

Livet MO, Moncla A, Delobel B, Croquette MF, Philip N, Vallée L. Livet MO, et al. Among authors: delobel b. Arch Pediatr. 1997 Dec;4(12):1231-7. doi: 10.1016/s0929-693x(97)82615-2. Arch Pediatr. 1997. PMID: 9538429 French.

7

[Unusual mechanism in Prader-Willi syndrome: incidence in genetic counseling].

Klosowski S, Delobel B, Morisot C, Kongolo G, Biancalana V, Thelliez P, Djebara A, Croquette MF, Deroubaix P. Klosowski S, et al. Among authors: delobel b. Arch Pediatr. 1998 Aug;5(8):934-5. doi: 10.1016/s0929-693x(98)80208-x. Arch Pediatr. 1998. PMID: 9759307 French. No abstract available.

8

Severe phenotype resulting from an active ring X chromosome in a female with a complex karyotype: characterisation and replication study.

Stavropoulou C, Mignon C, Delobel B, Moncla A, Depetris D, Croquette MF, Mattei MG. Stavropoulou C, et al. Among authors: delobel b. J Med Genet. 1998 Nov;35(11):932-8. doi: 10.1136/jmg.35.11.932. J Med Genet. 1998. PMID: 9832041 Free PMC article.

9

Identification and molecular characterization of a small 11q23.3 de novo duplication in a patient with Rett syndrome manifestations.

Delobel B, Delannoy V, Pini G, Zapella M, Tardieu M, Vallée L, Croquette MF. Delobel B, et al. Am J Med Genet. 1998 Nov 16;80(3):273-80. Am J Med Genet. 1998. PMID: 9843053

10

[ Head and truncal abnormalities and secondary clinical aspects of 22q11 microdeletion. A series of 111 patients].

Brevière GM, Croquette MF, Delobel B, Pellerin P, Rey C. Brevière GM, et al. Among authors: delobel b. Arch Pediatr. 1999;6 Suppl 2:305s-307s. doi: 10.1016/s0929-693x(99)80448-5. Arch Pediatr. 1999. PMID: 10370516 French. No abstract available.

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