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J A Crolla

Showing results (21-30 of 78) with videos related to

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Genetical Research|February 1, 1990
The induction of tail malformations in trisomy 16 mouse fetuses heterozygous for the curly tail recessive geneJ A Crolla, S K Lakeman, M J Seller
Humangenetik|January 1, 1974
A familial reciprocal translocation between three chromosomesM R Creasy, J A Crolla, M G Daker
Journal of Medical Genetics|October 1, 1992
A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in manJ A Crolla, N R Dennis, P A Jacobs
Clinical Genetics|October 1, 1994
Mixed gonadal dysgenesis and cell line differentiation. Case presentation and literature reviewI D Sugarman, J A Crolla, P S Malone
Development (Cambridge, England)|October 1, 1988
Prevention of spinal neural tube defects in the mouse embryo by growth retardation during neurulationA J Copp, J A Crolla, F A Brook
Cytogenetics and Cell Genetics|January 1, 1989
Meiosis in trisomic female mice with Robertsonian translocations. I. Prophase pairingP E Polani, J A Crolla, H J Roberts
Journal of Medical Genetics|March 1, 1996
X inactivation analysis in a female with hypomelanosis of Ito associated with a balanced X;17 translocation: evidence for functional disomy of XpE Hatchwell, D Robinson, J A Crolla, et al.
American Journal of Medical Genetics|March 3, 1998
FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new casesJ A Crolla, F Long, H Rivera, et al.
Journal of Medical Genetics|November 1, 1995
A familial Xp+ chromosome, dup (Xq26.3-->qter)A I Vasquez, H Rivera, L Bobadilla, et al.
Journal of Medical Genetics|February 25, 1998
Intrachromosomal triplication of distal 7pH Rivera, L Bobadilla, A Rolon, et al.
Pageof 8

Showing results (21-30 of 78) with videos related to

Sort By:
Pageof 8
Genetical Research|February 1, 1990
The induction of tail malformations in trisomy 16 mouse fetuses heterozygous for the curly tail recessive geneJ A Crolla, S K Lakeman, M J Seller
Humangenetik|January 1, 1974
A familial reciprocal translocation between three chromosomesM R Creasy, J A Crolla, M G Daker
Journal of Medical Genetics|October 1, 1992
A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in manJ A Crolla, N R Dennis, P A Jacobs
Clinical Genetics|October 1, 1994
Mixed gonadal dysgenesis and cell line differentiation. Case presentation and literature reviewI D Sugarman, J A Crolla, P S Malone
Development (Cambridge, England)|October 1, 1988
Prevention of spinal neural tube defects in the mouse embryo by growth retardation during neurulationA J Copp, J A Crolla, F A Brook
Cytogenetics and Cell Genetics|January 1, 1989
Meiosis in trisomic female mice with Robertsonian translocations. I. Prophase pairingP E Polani, J A Crolla, H J Roberts
Journal of Medical Genetics|March 1, 1996
X inactivation analysis in a female with hypomelanosis of Ito associated with a balanced X;17 translocation: evidence for functional disomy of XpE Hatchwell, D Robinson, J A Crolla, et al.
American Journal of Medical Genetics|March 3, 1998
FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new casesJ A Crolla, F Long, H Rivera, et al.
Journal of Medical Genetics|November 1, 1995
A familial Xp+ chromosome, dup (Xq26.3-->qter)A I Vasquez, H Rivera, L Bobadilla, et al.
Journal of Medical Genetics|February 25, 1998
Intrachromosomal triplication of distal 7pH Rivera, L Bobadilla, A Rolon, et al.
Pageof 8