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The Pharos of Alpha Omega Alpha-Honor Medical Society. Alpha Omega Alpha
|
January 1, 1989
Counseling the individual: genetic concerns
J L Gorski
American Journal of Medical Genetics
|
November 14, 2000
In memoriam: James V. Neel, 1915-2000
J 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 mosaicism
J 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 syndrome
P Hedera, J L Gorski
Journal of Medical Genetics
|
August 10, 2001
Ocular malformations, postaxial polydactyly, and delayed intramembranous ossification: a new autosomal dominant condition
D M Martin, J L Gorski
Journal of Medical Genetics
|
September 1, 1993
Nager acrofacial dysostosis
M 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 syndrome
N G Pasteris, J L Gorski
Seminars in Dermatology
|
September 1, 1993
The molecular genetics of incontinentia pigmenti
J 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 homologues
N 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) locus
E N Burright, J L Gorski
Page
of 6
Search research articles
Search
Showing results (1-10 of 53) with videos related to
Sort By:
Page
of 6
The Pharos of Alpha Omega Alpha-Honor Medical Society. Alpha Omega Alpha
|
January 1, 1989
Counseling the individual: genetic concerns
J L Gorski
American Journal of Medical Genetics
|
November 14, 2000
In memoriam: James V. Neel, 1915-2000
J 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 mosaicism
J 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 syndrome
P Hedera, J L Gorski
Journal of Medical Genetics
|
August 10, 2001
Ocular malformations, postaxial polydactyly, and delayed intramembranous ossification: a new autosomal dominant condition
D M Martin, J L Gorski
Journal of Medical Genetics
|
September 1, 1993
Nager acrofacial dysostosis
M 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 syndrome
N G Pasteris, J L Gorski
Seminars in Dermatology
|
September 1, 1993
The molecular genetics of incontinentia pigmenti
J 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 homologues
N 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) locus
E N Burright, J L Gorski
Page
of 6