Philip N - Search Results

1

[Microdeletion of the chromosome 22q11 in children: apropos of a series of 49 patients].

Levy-Mozziconacci A, Lacombe D, Leheup B, Wernert F, Rouault F, Philip N. Levy-Mozziconacci A, et al. Among authors: philip n. Arch Pediatr. 1996 Aug;3(8):761-8. doi: 10.1016/0929-693x(96)82157-9. Arch Pediatr. 1996. PMID: 8998528 French.

2

[The Beals-Hecht syndrome (congenital contractural arachnodactyly) revealed in a neonate].

Philip N, Garcia-Meric P, Wernert F. Philip N, et al. Pediatrie. 1988;43(7):609-12. Pediatrie. 1988. PMID: 3200664 French.

3

[Balanced chromosome rearrangements with abnormal phenotype].

Philip N, Mattei MG, Pellissier MC, Mattei JF, Giraud F. Philip N, et al. J Genet Hum. 1988 Jan;36(1-2):37-43. J Genet Hum. 1988. PMID: 3379378 French.

4

Clinical and molecular study of DiGeorge sequence.

Levy-Mozziconacci A, Wernert F, Scambler P, Rouault F, Metras D, Kreitman B, Depetris D, Mattei MG, Philip N. Levy-Mozziconacci A, et al. Among authors: philip n. Eur J Pediatr. 1994 Nov;153(11):813-20. doi: 10.1007/BF01972889. Eur J Pediatr. 1994. PMID: 7843195

5

Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome.

Levy A, Demczuk S, Aurias A, Depétris D, Mattei MG, Philip N. Levy A, et al. Among authors: philip n. Hum Mol Genet. 1995 Dec;4(12):2417-9. doi: 10.1093/hmg/4.12.2417. Hum Mol Genet. 1995. PMID: 8634722 No abstract available.

6

i(18q) in amniotic and fetal cells with a normal karyotype in direct chorionic villus sampling: cytogenetics and pathology.

Levy-Mozziconacci A, Piquet C, Scheiner C, Adrai J, Potier A, Pelissier MC, Philip N. Levy-Mozziconacci A, et al. Among authors: philip n. Prenat Diagn. 1996 Dec;16(12):1156-9. doi: 10.1002/(SICI)1097-0223(199612)16:12<1156::AID-PD13>3.0.CO;2-K. Prenat Diagn. 1996. PMID: 8994254

7

Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: a new component manifestation of deletion 22q11?

Lévy A, Michel G, Lemerrer M, Philip N. Lévy A, et al. Among authors: philip n. Am J Med Genet. 1997 Apr 14;69(4):356-9. doi: 10.1002/(sici)1096-8628(19970414)69:4<356::aid-ajmg4>3.0.co;2-j. Am J Med Genet. 1997. PMID: 9098482

8

Increased paternal age in CHARGE association.

Tellier AL, Lyonnet S, Cormier-Daire V, de Lonlay P, Abadie V, Baumann C, Bonneau D, Labrune P, Lacombe D, Le Merrer M, Nivelon A, Philip N, Briard ML, Munnich A. Tellier AL, et al. Among authors: philip n. Clin Genet. 1996 Dec;50(6):548-50. doi: 10.1111/j.1399-0004.1996.tb02736.x. Clin Genet. 1996. PMID: 9147897

9

Prenatal diagnosis of 22q11 microdeletion.

Levy-Mozziconacci A, Piquet C, Heurtevin PC, Philip N. Levy-Mozziconacci A, et al. Among authors: philip n. Prenat Diagn. 1997 Nov;17(11):1033-7. Prenat Diagn. 1997. PMID: 9399351 Clinical Trial.

10

[Smith-Magenis syndrome].

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

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