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

Autor: Tuerlings, JHAM, de France, HF, Hamers, A, Hordijk, R, Van Hemel, JO, Hansson, K, Hoovers, JMN, Madan, K, Van der Blij-Philipsen, M, Gerssen-Schoorl, KBJ, Kremer, JAM, Smeets, DFCM

Publikováno v: European Journal of Human Genetics, 6, 194-200. Nature Publishing Group
European Journal of Human Genetics, 6(3), 194-200. Nature Publishing Group

The chance of a male with severe oligozoospermia or azoospermia achieving a pregnancy has undergone a revolutionary increase with the introduction of the intracytoplasmic sperm injection technique (ICSI). However, since ICSI circumvents part of the n

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::273347ed0a2a317e480680bd5d7ad7a5
https://pure.eur.nl/en/publications/64d89b64-7dcd-4414-acf8-e9a4d65ccb27

The Dutch Uniform Multicenter Registration system for genetic disorders and malformation syndromes.

Autor: Zwamborn-Hanssen AM; Clinical Genetics Center Limburg, Maastricht, The Netherlands., Bijlsma JB, Hennekam EF, Lindhout D, Beemer FA, Bakker E, Kleijer WJ, de France HF, de Die-Smulders CE, Duran M, van Gennip AH, van Mens JT, Pearson PL, Mantel G, Verhage RE, Geraedts JP

Publikováno v: American journal of medical genetics [Am J Med Genet] 1997 Jun 27; Vol. 70 (4), pp. 444-7.

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

Autor: Christiaens GC; Department of Obstetrics and Gynaecology, University Hospital Utrecht, The Netherlands., Hagenaars AM, Akkerman C, De France HF

Publikováno v: Prenatal diagnosis [Prenat Diagn] 1996 May; Vol. 16 (5), pp. 437-42.

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

Autor: Verbraak FD; Department of Ophthalmogenetics, Netherlands Ophthalmic Research Institute, Amsterdam., Pogány K, Pilon JW, Mooy CM, de France HF, Hennekam RC, Bleeker-Wagemakers EM

Publikováno v: Ophthalmic paediatrics and genetics [Ophthalmic Paediatr Genet] 1992 Sep; Vol. 13 (3), pp. 165-70.

Duplication in chromosome 15q in a boy with the Prader-Willi syndrome; further cytogenetic confusion.

Autor: de France HF, Beemer FA, Ippel PF

Publikováno v: Clinical genetics [Clin Genet] 1984 Oct; Vol. 26 (4), pp. 379-82.