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N C Nevin

Showing results (111-120 of 223) with videos related to

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Irish Journal of Medical Science|August 13, 2016
A family with the testicular feminisation syndromeN C Nevin, J Willis, R A Magee, et al.
American Journal of Medical Genetics|February 7, 1998
Cleft lip and palate, hypertelorism, brachycephaly, flat facial profile, and congenital heart disease in three brothersN C Nevin, B G Craig, H C Mullholland, et al.
Journal of Medical Genetics|April 1, 1986
Duchenne muscular dystrophy in a female with a translocation involving Xp21N C Nevin, A E Hughes, M Calwell, et al.
American Journal of Medical Genetics|July 15, 1992
Orofaciodigital syndrome type IV: report of a patientN C Nevin, A C Mapee, V Mudenda, et al.
Irish Journal of Medical Science|November 1, 1976
A family with the testicular feminisation syndromeN C Nevin, J Willis, R A Magee, et al.
American Journal of Medical Genetics|July 1, 1994
Oral-facial-digital syndrome with retinal abnormalities: OFDS type IX. A further case reportN C Nevin, J Silvestri, D C Kernohan, et al.
Journal of Medical Genetics|February 1, 1990
Inverted tandem duplication of 8p12----p23.1 in a child with increased activity of glutathione reductaseN C Nevin, P J Morrison, J Jones, et al.
Clinical Genetics|November 1, 1983
Partial trisomy 16q in two boys resulting from a maternal translocation, t(15;16)(p12;q11)N C Nevin, W W Coffey, J Nevin, et al.
Journal of Medical Genetics|August 1, 1995
Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second familyN C Nevin, P S Thomas, D J Eedy, et al.
Clinical Otolaryngology and Allied Sciences|October 1, 1982
Tissue culture of surgically prepared temporalis fasciaA P Walby, A G Kerr, N C Nevin, et al.
Pageof 23

Showing results (111-120 of 223) with videos related to

Sort By:
Pageof 23
Irish Journal of Medical Science|August 13, 2016
A family with the testicular feminisation syndromeN C Nevin, J Willis, R A Magee, et al.
American Journal of Medical Genetics|February 7, 1998
Cleft lip and palate, hypertelorism, brachycephaly, flat facial profile, and congenital heart disease in three brothersN C Nevin, B G Craig, H C Mullholland, et al.
Journal of Medical Genetics|April 1, 1986
Duchenne muscular dystrophy in a female with a translocation involving Xp21N C Nevin, A E Hughes, M Calwell, et al.
American Journal of Medical Genetics|July 15, 1992
Orofaciodigital syndrome type IV: report of a patientN C Nevin, A C Mapee, V Mudenda, et al.
Irish Journal of Medical Science|November 1, 1976
A family with the testicular feminisation syndromeN C Nevin, J Willis, R A Magee, et al.
American Journal of Medical Genetics|July 1, 1994
Oral-facial-digital syndrome with retinal abnormalities: OFDS type IX. A further case reportN C Nevin, J Silvestri, D C Kernohan, et al.
Journal of Medical Genetics|February 1, 1990
Inverted tandem duplication of 8p12----p23.1 in a child with increased activity of glutathione reductaseN C Nevin, P J Morrison, J Jones, et al.
Clinical Genetics|November 1, 1983
Partial trisomy 16q in two boys resulting from a maternal translocation, t(15;16)(p12;q11)N C Nevin, W W Coffey, J Nevin, et al.
Journal of Medical Genetics|August 1, 1995
Anonychia and absence/hypoplasia of distal phalanges (Cooks syndrome): report of a second familyN C Nevin, P S Thomas, D J Eedy, et al.
Clinical Otolaryngology and Allied Sciences|October 1, 1982
Tissue culture of surgically prepared temporalis fasciaA P Walby, A G Kerr, N C Nevin, et al.
Pageof 23