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N H Robin

Showing results (31-40 of 61) with videos related to

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The Laryngoscope|May 19, 2001
Genetic testing and genetic counseling for deafness: the future is hereJ W Brunger, A L Matthews, R H Smith, et al.
American Journal of Medical Genetics|November 15, 2000
Adult with an interstitial deletion of chromosome 10 [del(10)(q25. 1q25.3)]: overlap with Coffin-Lowry syndromeS E McCandless, S Schwartz, S Morrison, et al.
American Journal of Medical Genetics|December 8, 1998
Nonpenetrance in FGFR3-associated coronal synostosis syndromeN H Robin, J A Scott, A R Cohen, et al.
American Journal of Medical Genetics|January 31, 1997
Clinical and locus heterogeneity in brachydactyly type CN H Robin, M Gunay-Aygun, A Polinkovsky, et al.
American Journal of Medical Genetics|November 1, 1993
New finding of Schinzel-Giedion syndrome: a case with a malignant sacrococcygeal teratomaN H Robin, K Grace, T G DeSouza, et al.
Clinical Genetics|December 1, 1993
De novo interstitial deletion of the long arm of chromosome 3: 46,XX,del(3)(q25.1q26.1)N H Robin, M Magnusson, D McDonald-McGinn, et al.
The Journal of Pediatrics|July 13, 2000
Serum alpha-fetoprotein levels in Beckwith-Wiedemann syndromeD B Everman, C Shuman, B Dzolganovski, et al.
Journal of Medical Genetics|February 12, 2002
A variant of osteogenesis imperfecta type IV with resolving kyphomelia is caused by a novel COL1A2 mutationM T Johnson, S Morrison, S Heeger, et al.
American Journal of Medical Genetics|September 20, 2001
Distal 5q deletion syndrome: phenotypic correlationsI A Schafer, N H Robin, J J Posch, et al.
American Journal of Medical Genetics|December 30, 1996
Syntelencephaly in an infant of a diabetic motherN H Robin, L M Ko, S Heeger, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
The Laryngoscope|May 19, 2001
Genetic testing and genetic counseling for deafness: the future is hereJ W Brunger, A L Matthews, R H Smith, et al.
American Journal of Medical Genetics|November 15, 2000
Adult with an interstitial deletion of chromosome 10 [del(10)(q25. 1q25.3)]: overlap with Coffin-Lowry syndromeS E McCandless, S Schwartz, S Morrison, et al.
American Journal of Medical Genetics|December 8, 1998
Nonpenetrance in FGFR3-associated coronal synostosis syndromeN H Robin, J A Scott, A R Cohen, et al.
American Journal of Medical Genetics|January 31, 1997
Clinical and locus heterogeneity in brachydactyly type CN H Robin, M Gunay-Aygun, A Polinkovsky, et al.
American Journal of Medical Genetics|November 1, 1993
New finding of Schinzel-Giedion syndrome: a case with a malignant sacrococcygeal teratomaN H Robin, K Grace, T G DeSouza, et al.
Clinical Genetics|December 1, 1993
De novo interstitial deletion of the long arm of chromosome 3: 46,XX,del(3)(q25.1q26.1)N H Robin, M Magnusson, D McDonald-McGinn, et al.
The Journal of Pediatrics|July 13, 2000
Serum alpha-fetoprotein levels in Beckwith-Wiedemann syndromeD B Everman, C Shuman, B Dzolganovski, et al.
Journal of Medical Genetics|February 12, 2002
A variant of osteogenesis imperfecta type IV with resolving kyphomelia is caused by a novel COL1A2 mutationM T Johnson, S Morrison, S Heeger, et al.
American Journal of Medical Genetics|September 20, 2001
Distal 5q deletion syndrome: phenotypic correlationsI A Schafer, N H Robin, J J Posch, et al.
American Journal of Medical Genetics|December 30, 1996
Syntelencephaly in an infant of a diabetic motherN H Robin, L M Ko, S Heeger, et al.
Pageof 7