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J Antich

Showing results (31-40 of 38) with videos related to

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The Journal of Orthopaedic and Sports Physical Therapy|January 1, 1986
Evaluation of knee extensor mechanism disorders: clinical presentation of 1 12 patients*T J Antich, C C Randall, R A Westbrook, et al.
Anales Espanoles De Pediatria|February 1, 1990
[Acromesomelic dysplasia. Report of case]M Iriondo Sanz, R Manzanares Bahi, G Pons Peradejordi, et al.
Human Molecular Genetics|January 1, 1994
A missense mutation (211His-->Arg) and a silent (160Thr) mutation within the rhodopsin gene in a spanish autosomal dominant retinitis pigmentosa familyC Reig, N Llecha, J Antich, et al.
Human Mutation|January 1, 1996
New mutation in the 3'-acceptor splice site of intron 4 in the rhodopsin gene associated with autosomal dominant retinitis pigmentosa in a Basque familyC Reig, A I Alvarez, I Tejada, et al.
Genomics|March 1, 1990
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequencesK Buiting, M Neumann, H J Lüdecke, et al.
Human Genetics|September 1, 1990
Genotyping of the Spanish cystic fibrosis population at the delta F508 mutation site and RFLP linked lociB Jaume-Roig, B Simon-Bouy, A Taillandier, et al.
Ophthalmic Genetics|June 1, 1995
A point mutation in the RDS-peripherin gene in a Spanish family with central areolar choroidal dystrophyC Reig, A Serra, E Gean, et al.
Anales Espanoles De Pediatria|June 1, 1991
[Pallister-Killian syndrome and 12p tetrasomy: increased LDH-B activity]J Antich Femenias, M P Briones Godino, M A Vilaseca Busca, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
The Journal of Orthopaedic and Sports Physical Therapy|January 1, 1986
Evaluation of knee extensor mechanism disorders: clinical presentation of 1 12 patients*T J Antich, C C Randall, R A Westbrook, et al.
Anales Espanoles De Pediatria|February 1, 1990
[Acromesomelic dysplasia. Report of case]M Iriondo Sanz, R Manzanares Bahi, G Pons Peradejordi, et al.
Human Molecular Genetics|January 1, 1994
A missense mutation (211His-->Arg) and a silent (160Thr) mutation within the rhodopsin gene in a spanish autosomal dominant retinitis pigmentosa familyC Reig, N Llecha, J Antich, et al.
Human Mutation|January 1, 1996
New mutation in the 3'-acceptor splice site of intron 4 in the rhodopsin gene associated with autosomal dominant retinitis pigmentosa in a Basque familyC Reig, A I Alvarez, I Tejada, et al.
Genomics|March 1, 1990
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequencesK Buiting, M Neumann, H J Lüdecke, et al.
Human Genetics|September 1, 1990
Genotyping of the Spanish cystic fibrosis population at the delta F508 mutation site and RFLP linked lociB Jaume-Roig, B Simon-Bouy, A Taillandier, et al.
Ophthalmic Genetics|June 1, 1995
A point mutation in the RDS-peripherin gene in a Spanish family with central areolar choroidal dystrophyC Reig, A Serra, E Gean, et al.
Anales Espanoles De Pediatria|June 1, 1991
[Pallister-Killian syndrome and 12p tetrasomy: increased LDH-B activity]J Antich Femenias, M P Briones Godino, M A Vilaseca Busca, et al.
Pageof 4