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S A Lynch

Showing results (21-30 of 88) with videos related to

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Irish Medical Journal|July 30, 2010
Sensorineural hearing loss in childrenR Wormald, L Viani, S A Lynch, et al.
Lancet (London, England)|July 6, 1996
Methylenetetrahydrofolate reductase and neural tube defectsC Papapetrou, S A Lynch, J Burn, et al.
Archives of Disease in Childhood|March 27, 2009
Bannayan-Riley-Ruvalcaba syndrome: a cause of extreme macrocephaly and neurodevelopmental delayN E Lynch, S A Lynch, J McMenamin, et al.
Clinical Dysmorphology|April 1, 1997
Absent nails, kinesogenic choreoathetosis, epilepsy and developmental delay--a new autosomal dominant disorder?S A Lynch, D Gardner-Medwin, J Burn, et al.
Rheumatology (Oxford, England)|March 11, 2005
Recurrence risk for psoriasis and psoriatic arthritis within sibshipsA Myers, L J Kay, S A Lynch, et al.
Journal of Medical Genetics|August 3, 2000
Autosomal dominant sacral agenesis: Currarino syndromeS A Lynch, Y Wang, T Strachan, et al.
Journal of Medical Genetics|March 1, 1995
Kabuki syndrome-like features in monozygotic twin boys with a pseudodicentric chromosome 13S A Lynch, K A Ashcroft, S Zwolinski, et al.
Diseases of Aquatic Organisms|September 28, 2018
Role of the intertidal predatory shore crab Carcinus maenas in transmission dynamics of ostreid herpesvirus-1 microvariantB E Bookelaar, A J O'Reilly, S A Lynch, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|May 1, 1986
Evaluating the effect of a breastfeeding consultant on the duration of breastfeedingS A Lynch, A M Koch, T G Hislop, et al.
Clinical Genetics|May 26, 2017
Novel COL4A2 variant in a large pedigree: Consequences and dilemmasM McGovern, O Flanagan, B Lynch, et al.
Pageof 9

Showing results (21-30 of 88) with videos related to

Sort By:
Pageof 9
Irish Medical Journal|July 30, 2010
Sensorineural hearing loss in childrenR Wormald, L Viani, S A Lynch, et al.
Lancet (London, England)|July 6, 1996
Methylenetetrahydrofolate reductase and neural tube defectsC Papapetrou, S A Lynch, J Burn, et al.
Archives of Disease in Childhood|March 27, 2009
Bannayan-Riley-Ruvalcaba syndrome: a cause of extreme macrocephaly and neurodevelopmental delayN E Lynch, S A Lynch, J McMenamin, et al.
Clinical Dysmorphology|April 1, 1997
Absent nails, kinesogenic choreoathetosis, epilepsy and developmental delay--a new autosomal dominant disorder?S A Lynch, D Gardner-Medwin, J Burn, et al.
Rheumatology (Oxford, England)|March 11, 2005
Recurrence risk for psoriasis and psoriatic arthritis within sibshipsA Myers, L J Kay, S A Lynch, et al.
Journal of Medical Genetics|August 3, 2000
Autosomal dominant sacral agenesis: Currarino syndromeS A Lynch, Y Wang, T Strachan, et al.
Journal of Medical Genetics|March 1, 1995
Kabuki syndrome-like features in monozygotic twin boys with a pseudodicentric chromosome 13S A Lynch, K A Ashcroft, S Zwolinski, et al.
Diseases of Aquatic Organisms|September 28, 2018
Role of the intertidal predatory shore crab Carcinus maenas in transmission dynamics of ostreid herpesvirus-1 microvariantB E Bookelaar, A J O'Reilly, S A Lynch, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|May 1, 1986
Evaluating the effect of a breastfeeding consultant on the duration of breastfeedingS A Lynch, A M Koch, T G Hislop, et al.
Clinical Genetics|May 26, 2017
Novel COL4A2 variant in a large pedigree: Consequences and dilemmasM McGovern, O Flanagan, B Lynch, et al.
Pageof 9