Kaplan J - Search Results

1

First-trimester prenatal diagnosis in quintuplets: a practical approach using step-by-step embryo reduction.

Dumez Y, Dommergues M, Lyonnet S, Tada K, Kaplan J, Mandelbrot L. Dumez Y, et al. Among authors: kaplan j. Prenat Diagn. 1991 Sep;11(9):737-40. doi: 10.1002/pd.1970110912. Prenat Diagn. 1991. PMID: 1788180

2

[Molecular genetics and prenatal diagnosis. Status and perspectives].

Munnich A, Lyonnet S, Kaplan J, Briard ML. Munnich A, et al. Among authors: kaplan j. Ann Pediatr (Paris). 1991 Dec;38(10):651-4. Ann Pediatr (Paris). 1991. PMID: 1772203 Review. French. No abstract available.

3

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: kaplan j. 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.

4

Genetic counselling, carrier detection, and prenatal diagnosis in hemophilia. A service experience.

Kaplan J, Chauvet ML, Briard ML, Gazengel C. Kaplan J, et al. Ann Genet. 1988;31(4):221-5. Ann Genet. 1988. PMID: 3265305

5

[Prenatal diagnosis of various hereditary blinding diseases].

Michel-Awad A, Kaplan J, Briard ML, Turleau C, de Grouchy J, Munnich A, Dufier JL, Frezal J. Michel-Awad A, et al. Among authors: kaplan j. Ophtalmologie. 1990 May-Jun;4(3):237-9. Ophtalmologie. 1990. PMID: 2250955 French.

6

[Genetic counseling in ornithine carbamoyltransferase deficiency].

Pelet A, Toumas E, Rabier D, Kaplan J, Kamoun P, Frezal J, Saudubray JM, Munnich A. Pelet A, et al. Among authors: kaplan j. Ann Biol Clin (Paris). 1988;46(7):455-9. Ann Biol Clin (Paris). 1988. PMID: 2903704 French.

7

[Evaluation of the risk in autosomal dominant diseases].

Kaplan J, Toutain A, Briard ML, Frézal J. Kaplan J, et al. J Genet Hum. 1988 Jun;36(3):265-74. J Genet Hum. 1988. PMID: 3411307 French.

8

[Retinitis pigmentosa].

Souied E, Kaplan J, Soubrane G, Coscas G. Souied E, et al. Among authors: kaplan j. J Fr Ophtalmol. 1997;20(6):461-86. J Fr Ophtalmol. 1997. PMID: 9296044 Review. French. No abstract available.

9

[Genetic counseling in neurofibromatosis. Apropos of a study of 53 families].

Toutain A, Kaplan J, Briard ML, Frézal J. Toutain A, et al. Among authors: kaplan j. J Genet Hum. 1988 Jun;36(3):163-71. J Genet Hum. 1988. PMID: 3137311 French.

10

Age-related macular degeneration in grandparents of patients with Stargardt disease: genetic study.

Souied EH, Ducroq D, Gerber S, Ghazi I, Rozet JM, Perrault I, Munnich A, Dufier JL, Coscas G, Soubrane G, Kaplan J. Souied EH, et al. Among authors: kaplan j. Am J Ophthalmol. 1999 Aug;128(2):173-8. doi: 10.1016/s0002-9394(99)00145-2. Am J Ophthalmol. 1999. PMID: 10458172

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