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Clinical Dysmorphology
|
October 1, 1994
Isolated macrodactyly or extremely localized Proteus syndrome?
Y van Bever, R C Hennekam
Clinical Genetics
|
May 1, 1995
Haspeslagh syndrome without severe mental retardation and pterygia?
Y van Bever, R C Hennekam
Human Genetics
|
June 1, 1997
Recombination in a balanced complex translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocations
K Madan, A W Nieuwint, Y van Bever
American Journal of Medical Genetics
|
October 28, 1996
Autosomal dominant familial radial luxation, carpal fusion and scapular dysplasia with variable heart defects
Y van Bever, P F Dijkstra, R C Hennekam
European Journal of Pediatrics
|
April 1, 1996
Acromicric dysplasia and geleophysic dysplasia: similarities and differences
R C Hennekam, Y van Bever, J W Oorthuys
American Journal of Medical Genetics
|
November 15, 1992
Oculo-auriculo-vertebral complex and uncommon associated anomalies: report on 8 unrelated Brazilian patients
Y van Bever, J J van den Ende, A Richieri-Costa
Genetic Counseling (Geneva, Switzerland)
|
November 5, 2014
Early prenatal disruption; a foetus with features of severe limb body wall sequence, body stalk anomaly and amniotic bands
S Zeidler, G G Oudesluijs, E M Schoonderwaldt, et al.
American Journal of Medical Genetics
|
February 15, 1992
Marden-Walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consanguineous parents
J J van den Ende, Y van Bever, E S Rodini, et al.
Clinical Genetics
|
May 10, 2013
A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the Netherlands
R van Minkelen, Y van Bever, J N R Kromosoeto, et al.
Molecular Syndromology
|
May 9, 2013
VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations
E Brosens, H Eussen, Y van Bever, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Clinical Dysmorphology
|
October 1, 1994
Isolated macrodactyly or extremely localized Proteus syndrome?
Y van Bever, R C Hennekam
Clinical Genetics
|
May 1, 1995
Haspeslagh syndrome without severe mental retardation and pterygia?
Y van Bever, R C Hennekam
Human Genetics
|
June 1, 1997
Recombination in a balanced complex translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocations
K Madan, A W Nieuwint, Y van Bever
American Journal of Medical Genetics
|
October 28, 1996
Autosomal dominant familial radial luxation, carpal fusion and scapular dysplasia with variable heart defects
Y van Bever, P F Dijkstra, R C Hennekam
European Journal of Pediatrics
|
April 1, 1996
Acromicric dysplasia and geleophysic dysplasia: similarities and differences
R C Hennekam, Y van Bever, J W Oorthuys
American Journal of Medical Genetics
|
November 15, 1992
Oculo-auriculo-vertebral complex and uncommon associated anomalies: report on 8 unrelated Brazilian patients
Y van Bever, J J van den Ende, A Richieri-Costa
Genetic Counseling (Geneva, Switzerland)
|
November 5, 2014
Early prenatal disruption; a foetus with features of severe limb body wall sequence, body stalk anomaly and amniotic bands
S Zeidler, G G Oudesluijs, E M Schoonderwaldt, et al.
American Journal of Medical Genetics
|
February 15, 1992
Marden-Walker-like syndrome without psychomotor retardation: report of a Brazilian girl born to consanguineous parents
J J van den Ende, Y van Bever, E S Rodini, et al.
Clinical Genetics
|
May 10, 2013
A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the Netherlands
R van Minkelen, Y van Bever, J N R Kromosoeto, et al.
Molecular Syndromology
|
May 9, 2013
VACTERL Association Etiology: The Impact of de novo and Rare Copy Number Variations
E Brosens, H Eussen, Y van Bever, et al.
Page
of 2