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N C Nevin

Showing results (141-150 of 223) with videos related to

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Archives of Disease in Childhood|August 26, 1998
Confidential inquiry into families with two siblings with cystic fibrosisP J Morrison, F J Stewart, A C Magee, et al.
American Journal of Medical Genetics|March 9, 1999
Melorheostosis in a family with autosomal dominant osteopoikilosisN C Nevin, P S Thomas, R I Davis, et al.
Journal of Medical Genetics|August 1, 1992
Linkage of epidermolysis bullosa simplex to keratin gene lociK E McKenna, A E Hughes, E A Bingham, et al.
Lancet (London, England)|August 5, 1998
Prevalence of tuberous sclerosis in UKP J Morrison, C H Shepherd, F J Stewart, et al.
Neuromuscular Disorders : NMD|January 1, 1996
The prevalence of inherited neuromuscular disease in Northern IrelandM I Hughes, E M Hicks, N C Nevin, et al.
Pediatric Research|September 1, 1979
Detection of cystic fibrosis protein by isoelectric focusing of serumG W Tully, G B Nevin, I R Young, et al.
Birth Defects Original Article Series|January 1, 1982
Norrie's diseaseS S Johnston, J E Hanna, N C Nevin, et al.
Prenatal Diagnosis|February 1, 1990
Early amniocentesis: experience of 222 consecutive patients, 1987-1988J Nevin, N C Nevin, J C Dornan, et al.
Clinical Genetics|September 4, 1998
De novo direct duplication 2 (p12-->p21) with paternally inherited pericentric inversion 2p11.2 2q12.2A C Magee, M W Humphreys, S McKee, et al.
American Journal of Medical Genetics|February 5, 1998
Ullrich-Turner syndrome: seven pregnancies in an apparent 45,X womanA C Magee, N C Nevin, M J Armstrong, et al.
Pageof 23

Showing results (141-150 of 223) with videos related to

Sort By:
Pageof 23
Archives of Disease in Childhood|August 26, 1998
Confidential inquiry into families with two siblings with cystic fibrosisP J Morrison, F J Stewart, A C Magee, et al.
American Journal of Medical Genetics|March 9, 1999
Melorheostosis in a family with autosomal dominant osteopoikilosisN C Nevin, P S Thomas, R I Davis, et al.
Journal of Medical Genetics|August 1, 1992
Linkage of epidermolysis bullosa simplex to keratin gene lociK E McKenna, A E Hughes, E A Bingham, et al.
Lancet (London, England)|August 5, 1998
Prevalence of tuberous sclerosis in UKP J Morrison, C H Shepherd, F J Stewart, et al.
Neuromuscular Disorders : NMD|January 1, 1996
The prevalence of inherited neuromuscular disease in Northern IrelandM I Hughes, E M Hicks, N C Nevin, et al.
Pediatric Research|September 1, 1979
Detection of cystic fibrosis protein by isoelectric focusing of serumG W Tully, G B Nevin, I R Young, et al.
Birth Defects Original Article Series|January 1, 1982
Norrie's diseaseS S Johnston, J E Hanna, N C Nevin, et al.
Prenatal Diagnosis|February 1, 1990
Early amniocentesis: experience of 222 consecutive patients, 1987-1988J Nevin, N C Nevin, J C Dornan, et al.
Clinical Genetics|September 4, 1998
De novo direct duplication 2 (p12-->p21) with paternally inherited pericentric inversion 2p11.2 2q12.2A C Magee, M W Humphreys, S McKee, et al.
American Journal of Medical Genetics|February 5, 1998
Ullrich-Turner syndrome: seven pregnancies in an apparent 45,X womanA C Magee, N C Nevin, M J Armstrong, et al.
Pageof 23