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O Hurko

Showing results (51-60 of 58) with videos related to

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American Journal of Ophthalmology|September 15, 1992
Ophthalmic involvement in myo-neuro-gastrointestinal encephalopathy syndromeA B Threlkeld, N R Miller, K C Golnik, et al.
American Journal of Medical Genetics|September 1, 1993
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by multicolor in situ hybridizationR V Lebo, L Martelli, Y Su, et al.
Nature Genetics|May 31, 2001
Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from ScotlandR E McGinnis, H Fox, P Yates, et al.
American Journal of Human Genetics|December 1, 1994
Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophyC J DiDonato, K Morgan, J D Carpten, et al.
Human Genetics|March 1, 1994
Linkage mapping of the spinal muscular atrophy geneA H Burghes, S E Ingraham, Z Kóte-Jarai, et al.
The Journal of Pediatrics|April 1, 1987
Cervicomedullary compression in young patients with achondroplasia: value of comprehensive neurologic and respiratory evaluationC S Reid, R E Pyeritz, S E Kopits, et al.
Pediatric Research|November 1, 1990
Heteroplasmy in chronic external ophthalmoplegia: clinical and molecular observationsO Hurko, D R Johns, S L Rutledge, et al.
American Journal of Medical Genetics|June 22, 1999
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3G A Bellus, M J Bamshad, K A Przylepa, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
American Journal of Ophthalmology|September 15, 1992
Ophthalmic involvement in myo-neuro-gastrointestinal encephalopathy syndromeA B Threlkeld, N R Miller, K C Golnik, et al.
American Journal of Medical Genetics|September 1, 1993
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by multicolor in situ hybridizationR V Lebo, L Martelli, Y Su, et al.
Nature Genetics|May 31, 2001
Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from ScotlandR E McGinnis, H Fox, P Yates, et al.
American Journal of Human Genetics|December 1, 1994
Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophyC J DiDonato, K Morgan, J D Carpten, et al.
Human Genetics|March 1, 1994
Linkage mapping of the spinal muscular atrophy geneA H Burghes, S E Ingraham, Z Kóte-Jarai, et al.
The Journal of Pediatrics|April 1, 1987
Cervicomedullary compression in young patients with achondroplasia: value of comprehensive neurologic and respiratory evaluationC S Reid, R E Pyeritz, S E Kopits, et al.
Pediatric Research|November 1, 1990
Heteroplasmy in chronic external ophthalmoplegia: clinical and molecular observationsO Hurko, D R Johns, S L Rutledge, et al.
American Journal of Medical Genetics|June 22, 1999
Severe achondroplasia with developmental delay and acanthosis nigricans (SADDAN): phenotypic analysis of a new skeletal dysplasia caused by a Lys650Met mutation in fibroblast growth factor receptor 3G A Bellus, M J Bamshad, K A Przylepa, et al.
Pageof 6