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American Journal of Medical Genetics. Part A
|
March 25, 2004
Re: clinical report by Ahmad et al. 14q(22) deletion in a familial case of anophthalmia with polydactyly
Carlos A Bacino
American Journal of Medical Genetics. Part A
|
April 29, 2010
Introductory comments on special section-genomic microduplications: When adding may equal subtracting
Carlos A Bacino, Sau-Wai Cheung
European Journal of Medical Genetics
|
June 17, 2014
Etiopathogenesis of equinovarus foot malformations
Carlos A Bacino, Jacqueline T Hecht
BMC Medical Genetics
|
March 26, 2004
A case of familial isolated hemihyperplasia
Heidi A Heilstedt, Carlos A Bacino
American Journal of Medical Genetics. Part A
|
April 29, 2010
Common recurrent microduplication syndromes: diagnosis and management in clinical practice
Jonathan S Berg, Lorraine Potocki, Carlos A Bacino
American Journal of Medical Genetics. Part A
|
September 25, 2004
Re: Familial cryptic translocation (2;17) ascertained through recurrent spontaneous abortions: Bruyere H, Rajcan-Separovic E, Doyle J, Pantzar T, Langlois S
Carlos A Bacino, Farideh Z Bischoff, Lisa G Shaffer
American Journal of Medical Genetics. Part A
|
November 5, 2011
A male newborn with VACTERL association and Fanconi anemia with a FANCB deletion detected by array comparative genomic hybridization (aCGH)
Luis A Umaña, Pilar Magoulas, Weimin Bi, et al.
American Journal of Medical Genetics. Part A
|
February 7, 2012
WDR62 missense mutation in a consanguineous family with primary microcephaly
Carlos A Bacino, Luis A Arriola, Joanna Wiszniewska, et al.
American Journal of Medical Genetics. Part A
|
October 16, 2010
Haploinsufficiency of the LIM domain containing preferred translocation partner in lipoma (LPP) gene in patients with tetralogy of Fallot and VACTERL association
Cammon B Arrington, Ankita Patel, Carlos A Bacino, et al.
American Journal of Medical Genetics. Part A
|
June 12, 2016
4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions
Weimin Bi, Sau-Wai Cheung, Amy M Breman, et al.
Page
of 17
Search research articles
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Showing results (1-10 of 162) with videos related to
Sort By:
Page
of 17
American Journal of Medical Genetics. Part A
|
March 25, 2004
Re: clinical report by Ahmad et al. 14q(22) deletion in a familial case of anophthalmia with polydactyly
Carlos A Bacino
American Journal of Medical Genetics. Part A
|
April 29, 2010
Introductory comments on special section-genomic microduplications: When adding may equal subtracting
Carlos A Bacino, Sau-Wai Cheung
European Journal of Medical Genetics
|
June 17, 2014
Etiopathogenesis of equinovarus foot malformations
Carlos A Bacino, Jacqueline T Hecht
BMC Medical Genetics
|
March 26, 2004
A case of familial isolated hemihyperplasia
Heidi A Heilstedt, Carlos A Bacino
American Journal of Medical Genetics. Part A
|
April 29, 2010
Common recurrent microduplication syndromes: diagnosis and management in clinical practice
Jonathan S Berg, Lorraine Potocki, Carlos A Bacino
American Journal of Medical Genetics. Part A
|
September 25, 2004
Re: Familial cryptic translocation (2;17) ascertained through recurrent spontaneous abortions: Bruyere H, Rajcan-Separovic E, Doyle J, Pantzar T, Langlois S
Carlos A Bacino, Farideh Z Bischoff, Lisa G Shaffer
American Journal of Medical Genetics. Part A
|
November 5, 2011
A male newborn with VACTERL association and Fanconi anemia with a FANCB deletion detected by array comparative genomic hybridization (aCGH)
Luis A Umaña, Pilar Magoulas, Weimin Bi, et al.
American Journal of Medical Genetics. Part A
|
February 7, 2012
WDR62 missense mutation in a consanguineous family with primary microcephaly
Carlos A Bacino, Luis A Arriola, Joanna Wiszniewska, et al.
American Journal of Medical Genetics. Part A
|
October 16, 2010
Haploinsufficiency of the LIM domain containing preferred translocation partner in lipoma (LPP) gene in patients with tetralogy of Fallot and VACTERL association
Cammon B Arrington, Ankita Patel, Carlos A Bacino, et al.
American Journal of Medical Genetics. Part A
|
June 12, 2016
4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions
Weimin Bi, Sau-Wai Cheung, Amy M Breman, et al.
Page
of 17