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Clinical genetics

Showing results (701-710 of 7,173) with videos related to

Pageof 718
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Clinical Genetics|May 10, 2012
The fragile X-associated tremor ataxia syndrome (FXTAS) in IndonesiaT I Winarni, F E P Mundhofir, A Ediati, et al.
Clinical Genetics|December 2, 2011
FOXG1 mutations in Japanese patients with the congenital variant of Rett syndromeS Takahashi, N Matsumoto, A Okayama, et al.
Clinical Genetics|August 1, 1990
Disomic balanced reciprocal translocationP L Wilmot, L R Shapiro, A C Casamassima
Clinical Genetics|August 1, 1990
Congenital tracheal stenosis in Pfeiffer syndromeP Stone, C L Trevenen, I Mitchell, et al.
Clinical Genetics|August 1, 1990
Spinal muscular atrophy type I combined with atrial septal defect in three sibsP Møller, N Moe, O D Saugstad, et al.
Clinical Genetics|November 19, 2011
Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamicsR De Filippis, L Pancrazi, K Bjørgo, et al.
Clinical Genetics|February 23, 2012
The Ehlers-Danlos syndrome, a disorder with many facesA De Paepe, F Malfait
Clinical Genetics|January 31, 2012
High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher diseaseB Bilir, Z Yapici, C Yalcinkaya, et al.
Clinical Genetics|February 17, 2012
MODY type 2 P59S GCK mutant: founder effect in South of ItalyM Delvecchio, O Ludovico, E Bellacchio, et al.
Clinical Genetics|February 17, 2012
Somatic mosaicism in a mother of two children with Pitt-Hopkins syndromeC V M Steinbusch, K E P van Roozendaal, D Tserpelis, et al.
Pageof 718

Showing results (701-710 of 7,173) with videos related to

Sort By:
Pageof 718
Clinical Genetics|May 10, 2012
The fragile X-associated tremor ataxia syndrome (FXTAS) in IndonesiaT I Winarni, F E P Mundhofir, A Ediati, et al.
Clinical Genetics|December 2, 2011
FOXG1 mutations in Japanese patients with the congenital variant of Rett syndromeS Takahashi, N Matsumoto, A Okayama, et al.
Clinical Genetics|August 1, 1990
Disomic balanced reciprocal translocationP L Wilmot, L R Shapiro, A C Casamassima
Clinical Genetics|August 1, 1990
Congenital tracheal stenosis in Pfeiffer syndromeP Stone, C L Trevenen, I Mitchell, et al.
Clinical Genetics|August 1, 1990
Spinal muscular atrophy type I combined with atrial septal defect in three sibsP Møller, N Moe, O D Saugstad, et al.
Clinical Genetics|November 19, 2011
Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamicsR De Filippis, L Pancrazi, K Bjørgo, et al.
Clinical Genetics|February 23, 2012
The Ehlers-Danlos syndrome, a disorder with many facesA De Paepe, F Malfait
Clinical Genetics|January 31, 2012
High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher diseaseB Bilir, Z Yapici, C Yalcinkaya, et al.
Clinical Genetics|February 17, 2012
MODY type 2 P59S GCK mutant: founder effect in South of ItalyM Delvecchio, O Ludovico, E Bellacchio, et al.
Clinical Genetics|February 17, 2012
Somatic mosaicism in a mother of two children with Pitt-Hopkins syndromeC V M Steinbusch, K E P van Roozendaal, D Tserpelis, et al.
Pageof 718