Tuerlings J - Search Results

1

Severe, non X-linked congenital microcephaly with absence of the pyramidal tracts in two siblings.

ten Donkelaar HJ, Wesseling P, Semmekrot BA, Liem KD, Tuerlings J, Cruysberg JR, de Wit PE. ten Donkelaar HJ, et al. Among authors: tuerlings j. Acta Neuropathol. 1999 Aug;98(2):203-11. doi: 10.1007/s004010051070. Acta Neuropathol. 1999. PMID: 10442561

2

Localization of the gene for X-linked Alport's syndrome.

Brunner H, Schröder C, van Bennekom C, Lambermon E, Tuerlings J, Menzel D, Olbing H, Monnens L, Wieringa B, Ropers HH. Brunner H, et al. Among authors: tuerlings j. Kidney Int. 1988 Oct;34(4):507-10. doi: 10.1038/ki.1988.210. Kidney Int. 1988. PMID: 3199669 Free article.

3

Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other Hand/Foot anomalies maps to human chromosome 3q27.

van Bokhoven H, Jung M, Smits AP, van Beersum S, Rüschendorf F, van Steensel M, Veenstra M, Tuerlings JH, Mariman EC, Brunner HG, Wienker TF, Reis A, Ropers HH, Hamel BC. van Bokhoven H, et al. Among authors: tuerlings jh. Am J Hum Genet. 1999 Feb;64(2):538-46. doi: 10.1086/302246. Am J Hum Genet. 1999. PMID: 9973291 Free PMC article.

4

Radial defects and testicular dysfunction: a new syndrome?

Tuerlings JH, Otten BJ, Hamilton CJ, Brunner HG. Tuerlings JH, et al. Clin Dysmorphol. 1999 Jul;8(3):203-5. Clin Dysmorphol. 1999. PMID: 10457855

5

Familial oligoasthenoteratozoospermia: evidence of autosomal dominant inheritance with sex-limited expression.

Tuerlings JH, van Golde RJ, Oudakker AR, Yntema HG, Kremer JA. Tuerlings JH, et al. Fertil Steril. 2002 Feb;77(2):415-8. doi: 10.1016/s0015-0282(01)02996-x. Fertil Steril. 2002. PMID: 11821108 Free article.

6

Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32).

Kroes HY, Tuerlings JH, Hordijk R, Folkers NR, ten Kate LP. Kroes HY, et al. Among authors: tuerlings jh. J Med Genet. 1994 Feb;31(2):156-8. doi: 10.1136/jmg.31.2.156. J Med Genet. 1994. PMID: 8182726 Free PMC article. Review.

7

Mutation frequency of cystic fibrosis transmembrane regulator is not increased in oligozoospermic male candidates for intracytoplasmic sperm injection.

Tuerlings JH, Mol B, Kremer JA, Looman M, Meuleman EJ, te Meerman GJ, Buys CH, Merkus HM, Scheffer H. Tuerlings JH, et al. Fertil Steril. 1998 May;69(5):899-903. doi: 10.1016/s0015-0282(98)00050-8. Fertil Steril. 1998. PMID: 9591500 Free article.

8

Down syndrome in the family: what to do when the karyotype of the proband is not available.

Tuerlings JH, Oosterwijk JC, ten Kate LP. Tuerlings JH, et al. Prenat Diagn. 1996 Jun;16(6):554-8. doi: 10.1002/(SICI)1097-0223(199606)16:6<554::AID-PD896>3.0.CO;2-I. Prenat Diagn. 1996. PMID: 8809898

9

Reproductive decisions of men with microdeletions of the Y chromosome: the role of genetic counselling.

Nap AW, Van Golde RJ, Tuerlings JH, De Sutter P, Pieters MH, Giltay JC, Kastrop PM, Braat DD, Kremer JA. Nap AW, et al. Among authors: tuerlings jh. Hum Reprod. 1999 Aug;14(8):2166-9. doi: 10.1093/humrep/14.8.2166. Hum Reprod. 1999. PMID: 10438445

10

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. Eur J Hum Genet. 1998 May-Jun;6(3):194-200. doi: 10.1038/sj.ejhg.5200193. Eur J Hum Genet. 1998. PMID: 9781022

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