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American Journal of Medical Genetics
|
May 20, 1999
Longitudinal changes in cognitive-behavioral levels in three children with FRAXE
G S Fisch, N J Carpenter, R Simensen, et al.
Case Reports in Genetics
|
June 7, 2017
Freeman-Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan Africa
A M Ali, R M Mbwasi, G Kinabo, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 5, 2001
Angelman syndrome in three adult patients with atypical presentation and severe neurological complications
G J Van Buggenhout, M J Descheemaeker, P Thiry, et al.
European Journal of Pediatrics
|
June 1, 1996
Additional congenital defects in anorectal malformations
E A Hassink, P N Rieu, B C Hamel, et al.
Atherosclerosis
|
August 23, 1996
Prevalence of familial mild hyperhomocysteinemia
D G Franken, G H Boers, H J Blom, et al.
Human Molecular Genetics
|
March 1, 1994
Six novel mutations in the alpha-galactosidase A gene in families with Fabry disease
J K Ploos van Amstel, R P Jansen, J G de Jong, et al.
American Journal of Medical Genetics
|
June 1, 1993
Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spots
H G Brunner, T Hulsebos, P M Steijlen, et al.
Human Genetics
|
April 1, 1994
Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family
F A Hol, M P Geurds, O Jensson, et al.
Neuropediatrics
|
December 1, 1996
Spinal muscular atrophy combined with congenital heart disease: a report of two cases
W M Mulleners, C M van Ravenswaay, F J Gabreëls, et al.
American Journal of Medical Genetics
|
July 12, 1996
Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings
B C Hamel, A P Smits, B J Otten, et al.
Page
of 13
Search research articles
Search
Showing results (51-60 of 129) with videos related to
Sort By:
Page
of 13
American Journal of Medical Genetics
|
May 20, 1999
Longitudinal changes in cognitive-behavioral levels in three children with FRAXE
G S Fisch, N J Carpenter, R Simensen, et al.
Case Reports in Genetics
|
June 7, 2017
Freeman-Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan Africa
A M Ali, R M Mbwasi, G Kinabo, et al.
Genetic Counseling (Geneva, Switzerland)
|
January 5, 2001
Angelman syndrome in three adult patients with atypical presentation and severe neurological complications
G J Van Buggenhout, M J Descheemaeker, P Thiry, et al.
European Journal of Pediatrics
|
June 1, 1996
Additional congenital defects in anorectal malformations
E A Hassink, P N Rieu, B C Hamel, et al.
Atherosclerosis
|
August 23, 1996
Prevalence of familial mild hyperhomocysteinemia
D G Franken, G H Boers, H J Blom, et al.
Human Molecular Genetics
|
March 1, 1994
Six novel mutations in the alpha-galactosidase A gene in families with Fabry disease
J K Ploos van Amstel, R P Jansen, J G de Jong, et al.
American Journal of Medical Genetics
|
June 1, 1993
Exclusion of the neurofibromatosis 1 locus in a family with inherited café-au-lait spots
H G Brunner, T Hulsebos, P M Steijlen, et al.
Human Genetics
|
April 1, 1994
Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family
F A Hol, M P Geurds, O Jensson, et al.
Neuropediatrics
|
December 1, 1996
Spinal muscular atrophy combined with congenital heart disease: a report of two cases
W M Mulleners, C M van Ravenswaay, F J Gabreëls, et al.
American Journal of Medical Genetics
|
July 12, 1996
Familial X-linked mental retardation and isolated growth hormone deficiency: clinical and molecular findings
B C Hamel, A P Smits, B J Otten, et al.
Page
of 13