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Genetic Counseling (Geneva, Switzerland)
|
November 5, 1999
11q- syndrome: three cases and a review of the literature
B Leegte, W S Kerstjens-Frederikse, K Deelstra, et al.
Human Genetics
|
January 1, 1992
Birth and population prevalence of Duchenne muscular dystrophy in The Netherlands
A J van Essen, H F Busch, G J te Meerman, et al.
Prenatal Diagnosis
|
October 30, 1998
Beta-glucuronidase deficiency as cause of recurrent hydrops fetalis: the first early prenatal diagnosis by chorionic villus sampling
H W Van Eyndhoven, H G Ter Brugge, A J Van Essen, et al.
American Journal of Medical Genetics. Part A
|
March 29, 2005
Malpuech syndrome: three patients and a review
W S Kerstjens-Frederikse, H G Brunner, C M L van Dael, et al.
American Journal of Medical Genetics
|
December 1, 1991
Cartilage hair hypoplasia, metaphyseal chondrodysplasia type McKusick: description of seven patients and review of the literature
I van der Burgt, A Haraldsson, J C Oosterwijk, et al.
Journal of Medical Genetics
|
April 16, 1999
A Hirschsprung disease locus at 22q11?
W S Kerstjens-Frederikse, R M Hofstra, A J van Essen, et al.
American Journal of Medical Genetics
|
October 6, 1999
Perlman syndrome: four additional cases and review
H T Henneveld, R A van Lingen, B C Hamel, et al.
Clinical Genetics
|
February 1, 1992
A boy with Poland anomaly and facio-auriculo-vertebral dysplasia
J M Cobben, A J van Essen, P C McParland, et al.
American Journal of Medical Genetics
|
August 1, 1989
Poland anomaly in mother and daughter
J M Cobben, P H Robinson, A J van Essen, et al.
American Journal of Medical Genetics
|
August 1, 1993
Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries
A J van Essen, C J Schoots, R A van Lingen, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 52) with videos related to
Sort By:
Page
of 6
Genetic Counseling (Geneva, Switzerland)
|
November 5, 1999
11q- syndrome: three cases and a review of the literature
B Leegte, W S Kerstjens-Frederikse, K Deelstra, et al.
Human Genetics
|
January 1, 1992
Birth and population prevalence of Duchenne muscular dystrophy in The Netherlands
A J van Essen, H F Busch, G J te Meerman, et al.
Prenatal Diagnosis
|
October 30, 1998
Beta-glucuronidase deficiency as cause of recurrent hydrops fetalis: the first early prenatal diagnosis by chorionic villus sampling
H W Van Eyndhoven, H G Ter Brugge, A J Van Essen, et al.
American Journal of Medical Genetics. Part A
|
March 29, 2005
Malpuech syndrome: three patients and a review
W S Kerstjens-Frederikse, H G Brunner, C M L van Dael, et al.
American Journal of Medical Genetics
|
December 1, 1991
Cartilage hair hypoplasia, metaphyseal chondrodysplasia type McKusick: description of seven patients and review of the literature
I van der Burgt, A Haraldsson, J C Oosterwijk, et al.
Journal of Medical Genetics
|
April 16, 1999
A Hirschsprung disease locus at 22q11?
W S Kerstjens-Frederikse, R M Hofstra, A J van Essen, et al.
American Journal of Medical Genetics
|
October 6, 1999
Perlman syndrome: four additional cases and review
H T Henneveld, R A van Lingen, B C Hamel, et al.
Clinical Genetics
|
February 1, 1992
A boy with Poland anomaly and facio-auriculo-vertebral dysplasia
J M Cobben, A J van Essen, P C McParland, et al.
American Journal of Medical Genetics
|
August 1, 1989
Poland anomaly in mother and daughter
J M Cobben, P H Robinson, A J van Essen, et al.
American Journal of Medical Genetics
|
August 1, 1993
Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries
A J van Essen, C J Schoots, R A van Lingen, et al.
Page
of 6