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A V Hing

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

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American Journal of Medical Genetics|February 15, 1993
Aase syndrome: novel radiographic featuresA V Hing, S B Dowton
American Journal of Human Genetics|August 1, 1993
VNTR and microsatellite polymorphisms within the subtelomeric region of 7qA V Hing, C Helms, H Donis-Keller
Clinical Genetics|February 1, 1992
A lethal syndrome resembling branchio-oculo-facial syndromeA V Hing, R Torack, S B Dowton
American Journal of Diseases of Children (1960)|July 1, 1989
Pulse oximetry in methemoglobinemiaM F Watcha, M T Connor, A V Hing
Journal of Medical Genetics|May 1, 1997
Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defectsS B Dowton, A V Hing, V Sheen-Kaniecki, et al.
American Journal of Medical Genetics|August 28, 1995
Linkage of preaxial polydactyly type 2 to 7q36A V Hing, C Helms, R Slaugh, et al.
American Journal of Medical Genetics|March 30, 1999
GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart diseaseT Pehlivan, B R Pober, M Brueckner, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 18, 2013
Clinical care in craniofacial microsomia: a review of current management recommendations and opportunities to advance researchC L Heike, A V Hing, C A Aspinall, et al.
Nature Genetics|November 1, 1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephalyE Belloni, M Muenke, E Roessler, et al.
Genomics|September 15, 1996
Mapping human telomere regions with YAC and P1 clones: chromosome-specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regionsA Vocero-Akbani, C Helms, J C Wang, et al.
Pageof 1

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

Sort By:
Pageof 1
American Journal of Medical Genetics|February 15, 1993
Aase syndrome: novel radiographic featuresA V Hing, S B Dowton
American Journal of Human Genetics|August 1, 1993
VNTR and microsatellite polymorphisms within the subtelomeric region of 7qA V Hing, C Helms, H Donis-Keller
Clinical Genetics|February 1, 1992
A lethal syndrome resembling branchio-oculo-facial syndromeA V Hing, R Torack, S B Dowton
American Journal of Diseases of Children (1960)|July 1, 1989
Pulse oximetry in methemoglobinemiaM F Watcha, M T Connor, A V Hing
Journal of Medical Genetics|May 1, 1997
Chromosome 18q22.2-->qter deletion and a congenital anomaly syndrome with multiple vertebral segmentation defectsS B Dowton, A V Hing, V Sheen-Kaniecki, et al.
American Journal of Medical Genetics|August 28, 1995
Linkage of preaxial polydactyly type 2 to 7q36A V Hing, C Helms, R Slaugh, et al.
American Journal of Medical Genetics|March 30, 1999
GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart diseaseT Pehlivan, B R Pober, M Brueckner, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 18, 2013
Clinical care in craniofacial microsomia: a review of current management recommendations and opportunities to advance researchC L Heike, A V Hing, C A Aspinall, et al.
Nature Genetics|November 1, 1996
Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephalyE Belloni, M Muenke, E Roessler, et al.
Genomics|September 15, 1996
Mapping human telomere regions with YAC and P1 clones: chromosome-specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regionsA Vocero-Akbani, C Helms, J C Wang, et al.
Pageof 1