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Clinical Genetics
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May 1, 1981
The hydrolethalus syndrome: delineation of a "new", lethal malformation syndrome based on 28 patients
R Salonen, R Herva, R Norio
Clinical Genetics
|
September 1, 1984
Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333)
F A Beemer, H F de France, I J Rosina-Angelista, et al.
Clinical Genetics
|
September 1, 1984
Occurrences of methylmalonic aciduria and Hartnup disorder in the same family
V E Shih, J T Coulombe, S K Wadman, et al.
Clinical Genetics
|
August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands
Stacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.
Clinical Genetics
|
December 1, 1987
Elevated 1,25-dihydroxyvitamin D and normocalcaemia in presumed familial Williams syndrome
J Knudtzon, L Aksnes, L A Akslen, et al.
Clinical Genetics
|
September 7, 2021
Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort
Amelie T van der Ven, Jessika Johannsen, Fanny Kortüm, et al.
Clinical Genetics
|
August 22, 2022
Psychiatric genetic counseling for people with copy number variants associated with psychiatric conditions
Emily Morris, Angela Inglis, Jehannine Austin
Clinical Genetics
|
April 1, 1987
A final word on the tricho-rhino-phalangeal syndromes
E M Bühler, U K Bühler, C Beutler, et al.
Clinical Genetics
|
May 20, 2021
Inflammatory factors, genetic variants, and predisposition for preterm birth
Joana Couceiro, Irina Matos, José João Mendes, et al.
Clinical Genetics
|
May 17, 2021
Current and experimental therapeutics for Fabry disease
Vanessa Castelli, Cosimo Andrea Stamerra, Michele d'Angelo, et al.
Page
of 718
Search research articles
Search
Showing results (371-380 of 7,173) with videos related to
Sort By:
Page
of 718
Clinical Genetics
|
May 1, 1981
The hydrolethalus syndrome: delineation of a "new", lethal malformation syndrome based on 28 patients
R Salonen, R Herva, R Norio
Clinical Genetics
|
September 1, 1984
Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333)
F A Beemer, H F de France, I J Rosina-Angelista, et al.
Clinical Genetics
|
September 1, 1984
Occurrences of methylmalonic aciduria and Hartnup disorder in the same family
V E Shih, J T Coulombe, S K Wadman, et al.
Clinical Genetics
|
August 31, 2021
Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands
Stacha F I Reumers, Corrie E Erasmus, Karlijn Bouman, et al.
Clinical Genetics
|
December 1, 1987
Elevated 1,25-dihydroxyvitamin D and normocalcaemia in presumed familial Williams syndrome
J Knudtzon, L Aksnes, L A Akslen, et al.
Clinical Genetics
|
September 7, 2021
Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort
Amelie T van der Ven, Jessika Johannsen, Fanny Kortüm, et al.
Clinical Genetics
|
August 22, 2022
Psychiatric genetic counseling for people with copy number variants associated with psychiatric conditions
Emily Morris, Angela Inglis, Jehannine Austin
Clinical Genetics
|
April 1, 1987
A final word on the tricho-rhino-phalangeal syndromes
E M Bühler, U K Bühler, C Beutler, et al.
Clinical Genetics
|
May 20, 2021
Inflammatory factors, genetic variants, and predisposition for preterm birth
Joana Couceiro, Irina Matos, José João Mendes, et al.
Clinical Genetics
|
May 17, 2021
Current and experimental therapeutics for Fabry disease
Vanessa Castelli, Cosimo Andrea Stamerra, Michele d'Angelo, et al.
Page
of 718