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M A Patton

Showing results (91-100 of 110) with videos related to

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American Journal of Medical Genetics|December 1, 1994
Small terminal deletions of the long arm of chromosome 2: two new casesA M Fisher, K H Ellis, C E Browne, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 9, 2002
Growth hormone therapy in Noonan's syndrome: non-cardiomyopathic congenital heart disease does not adversely affect growth improvementD C Brown, C E Macfarlane, W J McKenna, et al.
Heart (British Cardiac Society)|May 10, 2008
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the AmishK Zahka, K Kalidas, M A Simpson, et al.
Nature Genetics|September 18, 2001
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossiaC Braybrook, K Doudney, A C Marçano, et al.
American Journal of Human Genetics|July 1, 1994
Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1S W Scherer, P Poorkaj, T Allen, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2001
Growth hormone therapy and growth in children with Noonan's syndrome: results of 3 years' follow-upC E MacFarlane, D C Brown, L B Johnston, et al.
European Journal of Human Genetics : EJHG|December 31, 1997
Further delineation of the critical region for noonan syndrome on the long arm of chromosome 12A F Brady, C R Jamieson, I van der Burgt, et al.
Human Genetics|May 8, 2000
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22A R Afzal, A Rajab, C Fenske, et al.
Nature Genetics|December 1, 1994
Mapping a gene for Noonan syndrome to the long arm of chromosome 12C R Jamieson, I van der Burgt, A F Brady, et al.
American Journal of Medical Genetics|July 27, 2001
Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia lociH Patel, P E Hart, T Warner, et al.
Pageof 11

Showing results (91-100 of 110) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|December 1, 1994
Small terminal deletions of the long arm of chromosome 2: two new casesA M Fisher, K H Ellis, C E Browne, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 9, 2002
Growth hormone therapy in Noonan's syndrome: non-cardiomyopathic congenital heart disease does not adversely affect growth improvementD C Brown, C E Macfarlane, W J McKenna, et al.
Heart (British Cardiac Society)|May 10, 2008
Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the AmishK Zahka, K Kalidas, M A Simpson, et al.
Nature Genetics|September 18, 2001
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossiaC Braybrook, K Doudney, A C Marçano, et al.
American Journal of Human Genetics|July 1, 1994
Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1S W Scherer, P Poorkaj, T Allen, et al.
The Journal of Clinical Endocrinology and Metabolism|May 10, 2001
Growth hormone therapy and growth in children with Noonan's syndrome: results of 3 years' follow-upC E MacFarlane, D C Brown, L B Johnston, et al.
European Journal of Human Genetics : EJHG|December 31, 1997
Further delineation of the critical region for noonan syndrome on the long arm of chromosome 12A F Brady, C R Jamieson, I van der Burgt, et al.
Human Genetics|May 8, 2000
Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22A R Afzal, A Rajab, C Fenske, et al.
Nature Genetics|December 1, 1994
Mapping a gene for Noonan syndrome to the long arm of chromosome 12C R Jamieson, I van der Burgt, A F Brady, et al.
American Journal of Medical Genetics|July 27, 2001
Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia lociH Patel, P E Hart, T Warner, et al.
Pageof 11