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Irish Medical Journal
|
July 30, 2010
Sensorineural hearing loss in children
R Wormald, L Viani, S A Lynch, et al.
Lancet (London, England)
|
July 6, 1996
Methylenetetrahydrofolate reductase and neural tube defects
C 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 delay
N 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 sibships
A Myers, L J Kay, S A Lynch, et al.
Journal of Medical Genetics
|
August 3, 2000
Autosomal dominant sacral agenesis: Currarino syndrome
S 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 13
S 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 microvariant
B 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 breastfeeding
S A Lynch, A M Koch, T G Hislop, et al.
Clinical Genetics
|
May 26, 2017
Novel COL4A2 variant in a large pedigree: Consequences and dilemmas
M McGovern, O Flanagan, B Lynch, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 88) with videos related to
Sort By:
Page
of 9
Irish Medical Journal
|
July 30, 2010
Sensorineural hearing loss in children
R Wormald, L Viani, S A Lynch, et al.
Lancet (London, England)
|
July 6, 1996
Methylenetetrahydrofolate reductase and neural tube defects
C 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 delay
N 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 sibships
A Myers, L J Kay, S A Lynch, et al.
Journal of Medical Genetics
|
August 3, 2000
Autosomal dominant sacral agenesis: Currarino syndrome
S 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 13
S 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 microvariant
B 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 breastfeeding
S A Lynch, A M Koch, T G Hislop, et al.
Clinical Genetics
|
May 26, 2017
Novel COL4A2 variant in a large pedigree: Consequences and dilemmas
M McGovern, O Flanagan, B Lynch, et al.
Page
of 9