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C Govaerts

Showing results (31-40 of 35) with videos related to

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American Journal of Medical Genetics|May 1, 1994
Mosaic tetrasomy 8p in two patients: clinical data and review of the literatureC T Schrander-Stumpel, L C Govaerts, J J Engelen, et al.
Journal of Medical Genetics|February 1, 1993
The fragile X syndrome: no evidence for any recent mutationsA P Smits, J C Dreesen, J G Post, et al.
American Journal of Human Genetics|March 21, 2000
Familial syndromic esophageal atresia maps to 2p23-p24J Celli, E van Beusekom, R C Hennekam, et al.
Human Reproduction (Oxford, England)|April 1, 1999
Subfertile men with constitutive chromosome abnormalities do not necessarily refrain from intracytoplasmic sperm injection treatment: a follow-up study on 75 Dutch patientsJ C Giltay, P M Kastrop, J H Tuerlings, et al.
American Journal of Human Genetics|April 25, 2000
Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromereP E Warburton, M Dolled, R Mahmood, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
American Journal of Medical Genetics|May 1, 1994
Mosaic tetrasomy 8p in two patients: clinical data and review of the literatureC T Schrander-Stumpel, L C Govaerts, J J Engelen, et al.
Journal of Medical Genetics|February 1, 1993
The fragile X syndrome: no evidence for any recent mutationsA P Smits, J C Dreesen, J G Post, et al.
American Journal of Human Genetics|March 21, 2000
Familial syndromic esophageal atresia maps to 2p23-p24J Celli, E van Beusekom, R C Hennekam, et al.
Human Reproduction (Oxford, England)|April 1, 1999
Subfertile men with constitutive chromosome abnormalities do not necessarily refrain from intracytoplasmic sperm injection treatment: a follow-up study on 75 Dutch patientsJ C Giltay, P M Kastrop, J H Tuerlings, et al.
American Journal of Human Genetics|April 25, 2000
Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromereP E Warburton, M Dolled, R Mahmood, et al.
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