Tuerlings JH - Search Results

1

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.

2

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

3

[Down syndrome in the northeastern Netherlands; expectations and reality 1981-1986].

Cornel MC, Tuerlings JH, Breed AS, ten Kate LP. Cornel MC, et al. Among authors: tuerlings jh. Ned Tijdschr Geneeskd. 1990 Sep 22;134(38):1852-5. Ned Tijdschr Geneeskd. 1990. PMID: 2145518 Dutch.

4

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

5

Subfertile men with constitutive chromosome abnormalities do not necessarily refrain from intracytoplasmic sperm injection treatment: a follow-up study on 75 Dutch patients.

Giltay JC, Kastrop PM, Tuerlings JH, Kremer JA, Tiemessen CH, Gerssen-Schoorl KB, van der Veen F, de Vries J, Hordijk R, Hamers GJ, Hansson K, van der Blij-Philipsen M, Govaerts LC, Pieters MH, Madan K, Scheres JM. Giltay JC, et al. Among authors: tuerlings jh. Hum Reprod. 1999 Feb;14(2):318-20. doi: 10.1093/humrep/14.2.318. Hum Reprod. 1999. PMID: 10099971

6

Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries.

van Essen AJ, Schoots CJ, van Lingen RA, Mourits MJ, Tuerlings JH, Leegte B. van Essen AJ, et al. Among authors: tuerlings jh. Am J Med Genet. 1993 Aug 1;47(1):85-8. doi: 10.1002/ajmg.1320470117. Am J Med Genet. 1993. PMID: 8368259 Review.

7

Piebaldism in a mentally retarded girl with rare deletion of the long arm of chromosome 4.

Sijmons RH, Kristoffersson U, Tuerlings JH, Ljung R, Dijkhuis-Stoffelsma R, Breed AS. Sijmons RH, et al. Among authors: tuerlings jh. Pediatr Dermatol. 1993 Sep;10(3):235-9. doi: 10.1111/j.1525-1470.1993.tb00367.x. Pediatr Dermatol. 1993. PMID: 8415299

8

Diploid/triploid mosaicism in dysmorphic patients.

van de Laar I, Rabelink G, Hochstenbach R, Tuerlings J, Hoogeboom J, Giltay J. van de Laar I, et al. Clin Genet. 2002 Nov;62(5):376-82. doi: 10.1034/j.1399-0004.2002.620504.x. Clin Genet. 2002. PMID: 12431252 Review.

9

Cytogenetics of three cases of ANLL M2 and M4. Involvement of chromosomal region 8q22 in all three but 21q22 in only one.

Tuerlings J, Noordhoek L, Bosga-Bouwer A, Muis N, de Jong B. Tuerlings J, et al. Cancer Genet Cytogenet. 1990 Nov 1;50(1):103-7. doi: 10.1016/0165-4608(90)90243-4. Cancer Genet Cytogenet. 1990. PMID: 2253177

10

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.

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