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P J Goodfellow

Showing results (21-30 of 106) with videos related to

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Neurology|January 1, 1997
Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristicsJ L Elliott, J M Kwon, P J Goodfellow, et al.
Nucleic Acids Research|May 27, 1986
Three RFLPs recognized by an anonymous sequence localized to 21q11.2 [HGM8 D21S72]P J Goodfellow, A M Duncan, N E Simpson, et al.
American Journal of Human Genetics|May 1, 1990
Strong linkage disequilibrium between the XY274 polymorphism and the pseudoautosomal boundaryN Ellis, J Kidd, P J Goodfellow, et al.
Journal of Pediatric Surgery|June 29, 2000
16q loss of heterozygosity and microsatellite instability in Wilms' tumorJ E Mason, P J Goodfellow, P E Grundy, et al.
Gynecologic Oncology|February 1, 1996
Loss of heterozygosity of chromosome 3p sequences is an infrequent event in endometrial cancerM F Arlt, T J Herzog, D G Mutch, et al.
Human Molecular Genetics|October 1, 1995
Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2BY Kitamura, N Scavarda, S A Wells, et al.
Journal of Medical Genetics|May 1, 1989
Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile maleG C Beverstock, J D MacFarlane, H Veenema, et al.
Genomics|July 1, 1992
A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10J B Lichter, J Wu, D Miller, et al.
Genomics|June 1, 1992
Human repeat element-mediated PCR: cloning and mapping of chromosome 10 DNA markersA R Brooks-Wilson, D E Smailus, H U Weier, et al.
Cancer Letters|April 19, 1996
Mxi1 tumor suppressor gene is not mutated in primary pancreatic adenocarcinomaD Bartsch, S L Peiffer, Z Kaleem, et al.
Pageof 11

Showing results (21-30 of 106) with videos related to

Sort By:
Pageof 11
Neurology|January 1, 1997
Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristicsJ L Elliott, J M Kwon, P J Goodfellow, et al.
Nucleic Acids Research|May 27, 1986
Three RFLPs recognized by an anonymous sequence localized to 21q11.2 [HGM8 D21S72]P J Goodfellow, A M Duncan, N E Simpson, et al.
American Journal of Human Genetics|May 1, 1990
Strong linkage disequilibrium between the XY274 polymorphism and the pseudoautosomal boundaryN Ellis, J Kidd, P J Goodfellow, et al.
Journal of Pediatric Surgery|June 29, 2000
16q loss of heterozygosity and microsatellite instability in Wilms' tumorJ E Mason, P J Goodfellow, P E Grundy, et al.
Gynecologic Oncology|February 1, 1996
Loss of heterozygosity of chromosome 3p sequences is an infrequent event in endometrial cancerM F Arlt, T J Herzog, D G Mutch, et al.
Human Molecular Genetics|October 1, 1995
Two maternally derived missense mutations in the tyrosine kinase domain of the RET protooncogene in a patient with de novo MEN 2BY Kitamura, N Scavarda, S A Wells, et al.
Journal of Medical Genetics|May 1, 1989
Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile maleG C Beverstock, J D MacFarlane, H Veenema, et al.
Genomics|July 1, 1992
A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10J B Lichter, J Wu, D Miller, et al.
Genomics|June 1, 1992
Human repeat element-mediated PCR: cloning and mapping of chromosome 10 DNA markersA R Brooks-Wilson, D E Smailus, H U Weier, et al.
Cancer Letters|April 19, 1996
Mxi1 tumor suppressor gene is not mutated in primary pancreatic adenocarcinomaD Bartsch, S L Peiffer, Z Kaleem, et al.
Pageof 11