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A J Hoogeboom

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Clinical Genetics|December 1, 1983
The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritanceM J van de Vooren, M F Niermeijer, A J Hoogeboom
Journal of Medical Genetics|December 1, 1987
Interstitial del(13)(q21.3q31) associated with psychomotor retardation, eczema, and absent suck and swallowing reflexP J Peet, R R Pereira, J O Van Hemel, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 26, 2001
Prenatal diagnosis of type A1 brachydactylyN S den Hollander, A J Hoogeboom, M F Niermeijer, et al.
Human Genetics|January 1, 1980
Somatic cell hybridisation studies showing different gene mutations in Niemann-Pick variantsG T Besley, A J Hoogeboom, A Hoogeveen, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 10, 2002
Early prenatal sonographic diagnosis and follow-up of Jeune syndromeN S den Hollander, S G Robben, A J Hoogeboom, et al.
Obstetrics and Gynecology|March 1, 1985
Chromosome studies of 500 couples with two or more abortionsE S Sachs, M G Jahoda, J O Van Hemel, et al.
The Journal of Biological Chemistry|September 28, 2002
Mechanisms of copper incorporation into human ceruloplasminNathan E Hellman, Satoshi Kono, Grazia M Mancini, et al.
The Journal of Craniofacial Surgery|August 7, 1998
Pfeiffer's syndrome resulting from an S351C mutation in the fibroblast growth factor receptor-2 geneI M Mathijssen, J M Vaandrager, A J Hoogeboom, et al.
Human Genetics|February 1, 1991
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosisB A van Oost, P M van Zandvoort, W Tünte, et al.
American Journal of Medical Genetics|February 13, 2001
Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity aloneR J Galjaard, L I van der Ham, N A Posch, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Clinical Genetics|December 1, 1983
The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritanceM J van de Vooren, M F Niermeijer, A J Hoogeboom
Journal of Medical Genetics|December 1, 1987
Interstitial del(13)(q21.3q31) associated with psychomotor retardation, eczema, and absent suck and swallowing reflexP J Peet, R R Pereira, J O Van Hemel, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 26, 2001
Prenatal diagnosis of type A1 brachydactylyN S den Hollander, A J Hoogeboom, M F Niermeijer, et al.
Human Genetics|January 1, 1980
Somatic cell hybridisation studies showing different gene mutations in Niemann-Pick variantsG T Besley, A J Hoogeboom, A Hoogeveen, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 10, 2002
Early prenatal sonographic diagnosis and follow-up of Jeune syndromeN S den Hollander, S G Robben, A J Hoogeboom, et al.
Obstetrics and Gynecology|March 1, 1985
Chromosome studies of 500 couples with two or more abortionsE S Sachs, M G Jahoda, J O Van Hemel, et al.
The Journal of Biological Chemistry|September 28, 2002
Mechanisms of copper incorporation into human ceruloplasminNathan E Hellman, Satoshi Kono, Grazia M Mancini, et al.
The Journal of Craniofacial Surgery|August 7, 1998
Pfeiffer's syndrome resulting from an S351C mutation in the fibroblast growth factor receptor-2 geneI M Mathijssen, J M Vaandrager, A J Hoogeboom, et al.
Human Genetics|February 1, 1991
Linkage analysis in X-linked adrenoleukodystrophy and application in post- and prenatal diagnosisB A van Oost, P M van Zandvoort, W Tünte, et al.
American Journal of Medical Genetics|February 13, 2001
Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity aloneR J Galjaard, L I van der Ham, N A Posch, et al.
Pageof 2