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C E de Die-Smulders

Showing results (1-10 of 48) with videos related to

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American Journal of Medical Genetics|December 2, 1996
11Q duplication in a patient with Pitt-Rogers-Danks phenotypeC E de Die-Smulders, J J Engelen
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Unexpected molecular findings in 2 previously described brothers with Smith-Lemli-Opitz syndromeC E De Die-Smulders, H R Waterham, J P Fryns
Prenatal Diagnosis|September 22, 1998
Anencephaly in monozygotic twins and recurrence riskS G Frints, C E de Die-Smulders, T H Hasaart
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The lethal multiple pterygium syndrome: a nosological approachC E de Die-Smulders, C T Schrander-Stumpel, J P Fryns
European Journal of Pediatrics|August 1, 1992
McKusick-Kaufman syndrome: the diagnostic challenge of abdominal distension in the neonatal periodC Schaap, C E de Die-Smulders, R H Kuijten, et al.
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Management of sleeping problems in Wolf-Hirschhorn syndrome: a case studyL M Curfs, R Didden, S P Sikkema, et al.
Journal of Medical Genetics|October 1, 1991
Further evidence for the location of the BPES gene at 3q2C E de Die-Smulders, J J Engelen, J M Donk, et al.
American Journal of Medical Genetics|September 24, 1999
Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution bandingC E de Die-Smulders, J J Engelen, J C Albrechts, et al.
European Journal of Pediatrics|August 1, 1997
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletionK E Chandler, C E de Die-Smulders, J J Engelen, et al.
Journal of Medical Genetics|June 1, 1993
Severe intrauterine growth retardation, blepharophimosis, and cylindrical nose with midline groove: a new syndrome?C E de Die-Smulders, R P Droog, M van Dijk, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|December 2, 1996
11Q duplication in a patient with Pitt-Rogers-Danks phenotypeC E de Die-Smulders, J J Engelen
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Unexpected molecular findings in 2 previously described brothers with Smith-Lemli-Opitz syndromeC E De Die-Smulders, H R Waterham, J P Fryns
Prenatal Diagnosis|September 22, 1998
Anencephaly in monozygotic twins and recurrence riskS G Frints, C E de Die-Smulders, T H Hasaart
Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The lethal multiple pterygium syndrome: a nosological approachC E de Die-Smulders, C T Schrander-Stumpel, J P Fryns
European Journal of Pediatrics|August 1, 1992
McKusick-Kaufman syndrome: the diagnostic challenge of abdominal distension in the neonatal periodC Schaap, C E de Die-Smulders, R H Kuijten, et al.
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Management of sleeping problems in Wolf-Hirschhorn syndrome: a case studyL M Curfs, R Didden, S P Sikkema, et al.
Journal of Medical Genetics|October 1, 1991
Further evidence for the location of the BPES gene at 3q2C E de Die-Smulders, J J Engelen, J M Donk, et al.
American Journal of Medical Genetics|September 24, 1999
Detection of a cryptic translocation t(13;20)(q34;p13) in an unexplained case of MCA/MR: value of FISH over high resolution bandingC E de Die-Smulders, J J Engelen, J C Albrechts, et al.
European Journal of Pediatrics|August 1, 1997
Severe feeding problems and congenital laryngostenosis in a patient with 3q23 deletionK E Chandler, C E de Die-Smulders, J J Engelen, et al.
Journal of Medical Genetics|June 1, 1993
Severe intrauterine growth retardation, blepharophimosis, and cylindrical nose with midline groove: a new syndrome?C E de Die-Smulders, R P Droog, M van Dijk, et al.
Pageof 5