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J L Gorski

Showing results (1-10 of 53) with videos related to

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The Pharos of Alpha Omega Alpha-Honor Medical Society. Alpha Omega Alpha|January 1, 1989
Counseling the individual: genetic concernsJ L Gorski
American Journal of Medical Genetics|November 14, 2000
In memoriam: James V. Neel, 1915-2000J L Gorski
American Journal of Medical Genetics|September 1, 1991
Father-to-daughter transmission of focal dermal hypoplasia associated with nonrandom X-inactivation: support for X-linked inheritance and paternal X chromosome mosaicismJ L Gorski
American Journal of Medical Genetics|June 8, 2001
Retinitis pigmentosa, growth hormone deficiency, and acromelic skeletal dysplasia in two brothers: possible familial RHYNS syndromeP Hedera, J L Gorski
Journal of Medical Genetics|August 10, 2001
Ocular malformations, postaxial polydactyly, and delayed intramembranous ossification: a new autosomal dominant conditionD M Martin, J L Gorski
Journal of Medical Genetics|September 1, 1993
Nager acrofacial dysostosisM T McDonald, J L Gorski
Human Genetics|October 1, 1995
An intragenic TaqI polymorphism in the faciogenital dysplasia (FGD1) locus, the gene responsible for Aarskog syndromeN G Pasteris, J L Gorski
Seminars in Dermatology|September 1, 1993
The molecular genetics of incontinentia pigmentiJ L Gorski, E N Burright
Genomics|August 25, 1999
Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologuesN G Pasteris, J L Gorski
Nucleic Acids Research|January 11, 1993
Interspersed repetitive sequence (IRS)-PCR amplification of pulsed-field gel fractionated DNA to derive markers from the incontinentia pigmenti 1 (IP1) locusE N Burright, J L Gorski
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
The Pharos of Alpha Omega Alpha-Honor Medical Society. Alpha Omega Alpha|January 1, 1989
Counseling the individual: genetic concernsJ L Gorski
American Journal of Medical Genetics|November 14, 2000
In memoriam: James V. Neel, 1915-2000J L Gorski
American Journal of Medical Genetics|September 1, 1991
Father-to-daughter transmission of focal dermal hypoplasia associated with nonrandom X-inactivation: support for X-linked inheritance and paternal X chromosome mosaicismJ L Gorski
American Journal of Medical Genetics|June 8, 2001
Retinitis pigmentosa, growth hormone deficiency, and acromelic skeletal dysplasia in two brothers: possible familial RHYNS syndromeP Hedera, J L Gorski
Journal of Medical Genetics|August 10, 2001
Ocular malformations, postaxial polydactyly, and delayed intramembranous ossification: a new autosomal dominant conditionD M Martin, J L Gorski
Journal of Medical Genetics|September 1, 1993
Nager acrofacial dysostosisM T McDonald, J L Gorski
Human Genetics|October 1, 1995
An intragenic TaqI polymorphism in the faciogenital dysplasia (FGD1) locus, the gene responsible for Aarskog syndromeN G Pasteris, J L Gorski
Seminars in Dermatology|September 1, 1993
The molecular genetics of incontinentia pigmentiJ L Gorski, E N Burright
Genomics|August 25, 1999
Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologuesN G Pasteris, J L Gorski
Nucleic Acids Research|January 11, 1993
Interspersed repetitive sequence (IRS)-PCR amplification of pulsed-field gel fractionated DNA to derive markers from the incontinentia pigmenti 1 (IP1) locusE N Burright, J L Gorski
Pageof 6