Philip N - Search Results

1

Cerebrofaciothoracic dysplasia: a new family.

Philip N, Guala A, Moncla A, Monlouis M, Aymé S, Giraud F. Philip N, et al. J Med Genet. 1992 Jul;29(7):497-9. J Med Genet. 1992. PMID: 1640432 Free PMC article.

2

Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 16 non-Japanese cases.

Philip N, Meinecke P, David A, Dean J, Ayme S, Clark R, Gross-Kieselstein E, Hosenfeld D, Moncla A, Muller D, et al. Philip N, et al. Clin Dysmorphol. 1992 Apr;1(2):63-77. Clin Dysmorphol. 1992. PMID: 1285376

3

[Molecular biology in genetic counseling of Duchenne and Becker myopathy].

Philip N, Voelckel MA, Girardot L, Lambert JC, Moncla A, Mattei JF, Giraud F. Philip N, et al. Pediatrie. 1992;47(12):821-8. Pediatrie. 1992. PMID: 1338927 French.

4

Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.

Melki J, Abdelhak S, Burlet P, Raclin V, Kaplan J, Spiegel R, Gilgenkrantz S, Philip N, Chauvet ML, Dumez Y, et al. Melki J, et al. Among authors: philip n. J Med Genet. 1992 Mar;29(3):171-4. doi: 10.1136/jmg.29.3.171. J Med Genet. 1992. PMID: 1348092 Free PMC article.

5

Dysmorphology report: on the association of microcephaly and preaxial polydactyly. Another example of Howard-Young syndrome.

Collignon P, Philip N, Simonin G, Mattei JF, Giraud F. Collignon P, et al. Among authors: philip n. Genet Couns. 1992;3(4):221-2. Genet Couns. 1992. PMID: 1472358

6

Physical mapping of an Xq-proximal interstitial duplication in a male.

Muscatelli F, Verna JM, Philip N, Moncla A, Mattei MG, Mattei JF, Fontes M. Muscatelli F, et al. Among authors: philip n. Hum Genet. 1992 Mar;88(6):691-4. doi: 10.1007/BF02265299. Hum Genet. 1992. PMID: 1551675

7

Prenatal diagnosis of Fryns' syndrome.

Pellissier MC, Philip N, Potier A, Scheiner C, Aymé S, Mattei JF, Giraud F. Pellissier MC, et al. Among authors: philip n. Prenat Diagn. 1992 Apr;12(4):299-303. doi: 10.1002/pd.1970120410. Prenat Diagn. 1992. PMID: 1614987 Review.

8

Fragile X syndrome in an extended family with special reference to an affected male with Klinefelter syndrome.

Voelckel MA, Pellissier MC, Piquet C, N'Guyen C, Boccaccio I, Philip N, Mattei JF. Voelckel MA, et al. Among authors: n guyen c, philip n. Am J Med Genet. 1991 Feb-Mar;38(2-3):374-7. doi: 10.1002/ajmg.1320380243. Am J Med Genet. 1991. PMID: 1673314

9

[The usefulness of the level of alpha-fetoprotein (AFP) and electrophoresis of amniotic acetylcholinesterase for the detection of selected congenital malformations].

Lemonnier MC, Julian C, Aymé S, Philip N, Voeckel MA, Gamerre M, Mattéi JF. Lemonnier MC, et al. Among authors: philip n. J Gynecol Obstet Biol Reprod (Paris). 1990;19(3):280-4. J Gynecol Obstet Biol Reprod (Paris). 1990. PMID: 1693158 French.

10

Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study.

Verloes A, Aymé S, Gambarelli D, Gonzales M, Le Merrer M, Mulliez N, Philip N, Roume J. Verloes A, et al. Among authors: philip n. J Med Genet. 1991 May;28(5):297-303. doi: 10.1136/jmg.28.5.297. J Med Genet. 1991. PMID: 1865466 Free PMC article. Review.

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