Frederic J - Search Results

1

Mosaicism of 46,XX/47,XX,+9/47,XX,+?mar in the same amniotic fluid with apparent loss of one cell line after delivery.

Herens C, Pierquin G, Verloes A, Schaaps JP, Frederic J. Herens C, et al. Among authors: frederic j. Prenat Diagn. 1989 May;9(5):373-5. doi: 10.1002/pd.1970090513. Prenat Diagn. 1989. PMID: 2726702

2

Partial trisomy 20q due to paternal t(8;20) translocation. Case report and review of the literature.

Pierquin G, Herens C, Dodinval P, Frederic J, Weber I, Senterre J, Fryns JP. Pierquin G, et al. Among authors: frederic j. Clin Genet. 1988 May;33(5):386-9. doi: 10.1111/j.1399-0004.1988.tb03466.x. Clin Genet. 1988. PMID: 3288379 Review.

3

Chromosome 22 mosaic monosomy (46,XY/45,XY,-22).

Verloes A, Herens C, Lambotte C, Frederic J. Verloes A, et al. Among authors: frederic j. Ann Genet. 1987;30(3):178-9. Ann Genet. 1987. PMID: 3499857

4

[The fragile X syndrome in 1987. Recent findings and review of the problem].

Verloes A, Frederic J, Lambotte C. Verloes A, et al. Among authors: frederic j. Rev Med Liege. 1987 Nov 15;42(22):893-902. Rev Med Liege. 1987. PMID: 3321324 Review. French. No abstract available.

5

Noonan and Klinefelter syndromes in a child.

Verloes A, Guidi O, Frederic J, Lambotte C. Verloes A, et al. Among authors: frederic j. Am J Med Genet. 1987 Jul;27(3):727-8. doi: 10.1002/ajmg.1320270330. Am J Med Genet. 1987. PMID: 3631144 No abstract available.

6

[Prenatal diagnosis of chromosome abnormalities].

Lambotte C, Frederic J. Lambotte C, et al. Among authors: frederic j. Rev Med Liege. 1980 Dec 1;35(23):792-7. Rev Med Liege. 1980. PMID: 7010487 French. No abstract available.

7

[Deletion of the long arm of chromosome 5: karyotype 46, XY-46,XY, 5 q].

Lambotte C, Frederic J, Stainier L, Jovanovic M, Bauduin P. Lambotte C, et al. Among authors: frederic j. Acta Paediatr Belg. 1971;25(3):143-53. Acta Paediatr Belg. 1971. PMID: 5095924 French. No abstract available.

8

[C-G translocation: karyotype 46, XY,t(Cq-; Gq+): parents 46, XX and 46, XY].

Lambotte C, Carlier G, Frederic J, Keutgen J. Lambotte C, et al. Among authors: frederic j. Acta Paediatr Belg. 1971;25(2):119-26. Acta Paediatr Belg. 1971. PMID: 5565831 French. No abstract available.

9

[A case of mosaicism with a large, extra chromosome].

Hausman-Hagemeijer A, Frederic J, Dodinval P. Hausman-Hagemeijer A, et al. Among authors: frederic j. Humangenetik. 1966;2(1):52-62. doi: 10.1007/BF00285910. Humangenetik. 1966. PMID: 4958983 French. No abstract available.

10

[MULTIPLE CONGENITAL MALFORMATIONS IN 2 SISTERS. POSSIBLE ASSOCIATION WITH A CHROMOSOME 22 ABNORMALITY. PRELIMINARY NOTE].

FREDERIC J, MONARD Y, BONNET F, DODINVAL P. FREDERIC J, et al. Rev Med Liege. 1964 Apr 15;19:265-71. Rev Med Liege. 1964. PMID: 14144255 French. No abstract available.

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