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B D Hall

Showing results (201-210 of 208) with videos related to

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American Journal of Medical Genetics|May 2, 1997
Macrocephaly-cutis marmorata telangiectatica congenita: a distinct disorder with developmental delay and connective tissue abnormalitiesC A Moore, H V Toriello, D N Abuelo, et al.
Human Molecular Genetics|April 4, 2001
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombinationL Y Brown, S Odent, V David, et al.
American Journal of Medical Genetics|April 6, 1999
Acromelic frontonasal dysostosisS F Slaney, F R Goodman, B L Eilers-Walsman, et al.
Molecular Vision|May 13, 2010
Ocular manifestations of branchio-oculo-facial syndrome: report of a novel mutation and review of the literatureM S Al-Dosari, M Almazyad, L Al-Ebdi, et al.
American Journal of Medical Genetics|July 31, 2001
Meier-Gorlin syndrome: report of eight additional cases and reviewE M Bongers, J M Opitz, A Fryer, et al.
American Journal of Medical Genetics|December 23, 1999
Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: report of five new cases and reviewE K Pivnick, B Angle, R A Kaufman, et al.
American Journal of Human Genetics|August 1, 1996
Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of diseaseM H Ruttledge, A A Andermann, C M Phelan, et al.
Nature|May 24, 2019
Increase in CFC-11 emissions from eastern China based on atmospheric observationsM Rigby, S Park, T Saito, et al.
Pageof 21

Showing results (201-210 of 208) with videos related to

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Pageof 21
You have reached the last page of results.This site can display upto 208 results.
American Journal of Medical Genetics|May 2, 1997
Macrocephaly-cutis marmorata telangiectatica congenita: a distinct disorder with developmental delay and connective tissue abnormalitiesC A Moore, H V Toriello, D N Abuelo, et al.
Human Molecular Genetics|April 4, 2001
Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombinationL Y Brown, S Odent, V David, et al.
American Journal of Medical Genetics|April 6, 1999
Acromelic frontonasal dysostosisS F Slaney, F R Goodman, B L Eilers-Walsman, et al.
Molecular Vision|May 13, 2010
Ocular manifestations of branchio-oculo-facial syndrome: report of a novel mutation and review of the literatureM S Al-Dosari, M Almazyad, L Al-Ebdi, et al.
American Journal of Medical Genetics|July 31, 2001
Meier-Gorlin syndrome: report of eight additional cases and reviewE M Bongers, J M Opitz, A Fryer, et al.
American Journal of Medical Genetics|December 23, 1999
Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: report of five new cases and reviewE K Pivnick, B Angle, R A Kaufman, et al.
American Journal of Human Genetics|August 1, 1996
Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of diseaseM H Ruttledge, A A Andermann, C M Phelan, et al.
Nature|May 24, 2019
Increase in CFC-11 emissions from eastern China based on atmospheric observationsM Rigby, S Park, T Saito, et al.
Pageof 21