de France HF[au] - Search Results

Year	Number of Results
1974	1
1975	2
1976	2
1977	2
1978	1
1979	4
1981	1
1984	3
1985	2
1989	1
1992	1
1994	1
1996	1
1997	2
1998	1
2023	0

1

Partial trisomy 10q: a recognizable syndrome.

Klep-de Pater JM, Bijlsma JB, de France HF, Leschot NJ, Duijndam-van den Berge M, van Hemel JO. Klep-de Pater JM, et al. Among authors: de france hf. Hum Genet. 1979 Jan 19;46(1):29-40. doi: 10.1007/BF00278899. Hum Genet. 1979. PMID: 429004

2

Intracytoplasmic sperm injection (ICSI) and chromosomally abnormal spermatozoa.

In't Veld PA, Broekmans FJ, de France HF, Pearson PL, Pieters MH, van Kooij RJ. In't Veld PA, et al. Among authors: de france hf. Hum Reprod. 1997 Apr;12(4):752-4. doi: 10.1093/humrep/12.4.752. Hum Reprod. 1997. PMID: 9159437 Free article.

3

Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience.

Tuerlings JH, de France HF, Hamers A, Hordijk R, Van Hemel JO, Hansson K, Hoovers JM, Madan K, Van der Blij-Philipsen M, Gerssen-Schoorl KB, Kremer JA, Smeets DF. Tuerlings JH, et al. Among authors: de france hf. Eur J Hum Genet. 1998 May-Jun;6(3):194-200. doi: 10.1038/sj.ejhg.5200193. Eur J Hum Genet. 1998. PMID: 9781022

4

Automated selection of metaphase cells by quality.

van den Berg HT, de France HF, Habbema JD, Raatgever JW. van den Berg HT, et al. Among authors: de france hf. Cytometry. 1981 May;1(6):363-72. doi: 10.1002/cyto.990010602. Cytometry. 1981. PMID: 7023885 Free article.

5

Interstitial deletion of the long arm of chromosome 11.

Klep-de Pater JM, de France HF, Bijlsma JB. Klep-de Pater JM, et al. Among authors: de france hf. J Med Genet. 1985 Jun;22(3):224-6. doi: 10.1136/jmg.22.3.224. J Med Genet. 1985. PMID: 4009645 Free PMC article.

6

Are Down syndrome fetuses detected through maternal serum screening similar to those remaining undetected?

Christiaens GC, Hagenaars AM, Akkerman C, De France HF. Christiaens GC, et al. Among authors: de france hf. Prenat Diagn. 1996 May;16(5):437-42. doi: 10.1002/(SICI)1097-0223(199605)16:5<437::AID-PD889>3.0.CO;2-I. Prenat Diagn. 1996. PMID: 8844002

7

A third case of de novo partial trisomy 4p.

Oorthuys JW, Gerssen-Schoorl KB, de Pater JM, de France HF. Oorthuys JW, et al. Among authors: de france hf. J Med Genet. 1989 May;26(5):344-5. doi: 10.1136/jmg.26.5.344. J Med Genet. 1989. PMID: 2732997 Free PMC article. No abstract available.

8

Trisomy 10 mosaicism in a newborn boy; delineation of the syndrome.

de France HF, Beemer FA, Senders RC, Schaminée-Main SC. de France HF, et al. Clin Genet. 1985 Jan;27(1):92-6. doi: 10.1111/j.1399-0004.1985.tb00190.x. Clin Genet. 1985. PMID: 3978842

9

Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?

Breuning MH, Bijlsma JB, de France HF. Breuning MH, et al. Among authors: de france hf. Hum Genet. 1977 Aug 31;38(1):7-13. doi: 10.1007/BF00295802. Hum Genet. 1977. PMID: 903156

10

Congenital glaucoma in a child with partial 1q duplication and 9p deletion.

Verbraak FD, Pogány K, Pilon JW, Mooy CM, de France HF, Hennekam RC, Bleeker-Wagemakers EM. Verbraak FD, et al. Among authors: de france hf. Ophthalmic Paediatr Genet. 1992 Sep;13(3):165-70. doi: 10.3109/13816819209046485. Ophthalmic Paediatr Genet. 1992. PMID: 1484694

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