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H H Ardinger

Showing results (1-10 of 15) with videos related to

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Journal of Craniofacial Genetics and Developmental Biology|January 1, 1988
Microcephaly in familial holoprosencephalyH H Ardinger, J A Bartley
Archives of Neurology|August 1, 1986
Hypomelanosis of Ito. Wood's light and magnetic resonance imaging as diagnostic measuresH H Ardinger, W E Bell
American Journal of Medical Genetics|May 1, 1987
Association of neural tube defects with omphalocele in chromosomally normal fetusesH H Ardinger, R A Williamson, S Grant
American Family Physician|March 8, 2000
Identification and evaluation of mental retardationD K Daily, H H Ardinger, G E Holmes
Clinical Genetics|June 1, 1987
Trisomy 2q and monosomy 11q in the same individual: the importance of considering the deleted segmentH H Ardinger, S R Patil, W J Rhead
American Journal of Medical Genetics|December 1, 1984
Börjeson-Forssman-Lehmann syndrome: further delineation in five casesH H Ardinger, J W Hanson, H U Zellweger
American Journal of Medical Genetics|January 31, 1997
Cardiovascular malformations in Smith-Lemli-Opitz syndromeA E Lin, H H Ardinger, R H Ardinger, et al.
American Journal of Human Genetics|September 1, 1989
Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palateH H Ardinger, K H Buetow, G I Bell, et al.
American Journal of Medical Genetics|December 1, 1989
Linkage localization of Börjeson-Forssman-Lehmann syndromeK D Mathews, H H Ardinger, D Y Nishimura, et al.
American Journal of Human Genetics|October 1, 1993
Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO)R Shiang, A C Lidral, H H Ardinger, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Craniofacial Genetics and Developmental Biology|January 1, 1988
Microcephaly in familial holoprosencephalyH H Ardinger, J A Bartley
Archives of Neurology|August 1, 1986
Hypomelanosis of Ito. Wood's light and magnetic resonance imaging as diagnostic measuresH H Ardinger, W E Bell
American Journal of Medical Genetics|May 1, 1987
Association of neural tube defects with omphalocele in chromosomally normal fetusesH H Ardinger, R A Williamson, S Grant
American Family Physician|March 8, 2000
Identification and evaluation of mental retardationD K Daily, H H Ardinger, G E Holmes
Clinical Genetics|June 1, 1987
Trisomy 2q and monosomy 11q in the same individual: the importance of considering the deleted segmentH H Ardinger, S R Patil, W J Rhead
American Journal of Medical Genetics|December 1, 1984
Börjeson-Forssman-Lehmann syndrome: further delineation in five casesH H Ardinger, J W Hanson, H U Zellweger
American Journal of Medical Genetics|January 31, 1997
Cardiovascular malformations in Smith-Lemli-Opitz syndromeA E Lin, H H Ardinger, R H Ardinger, et al.
American Journal of Human Genetics|September 1, 1989
Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palateH H Ardinger, K H Buetow, G I Bell, et al.
American Journal of Medical Genetics|December 1, 1989
Linkage localization of Börjeson-Forssman-Lehmann syndromeK D Mathews, H H Ardinger, D Y Nishimura, et al.
American Journal of Human Genetics|October 1, 1993
Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO)R Shiang, A C Lidral, H H Ardinger, et al.
Pageof 2