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N O Dávalos

Showing results (1-10 of 7) with videos related to

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Clinical Dysmorphology|July 19, 2003
Myhre syndrome: first female caseN O Dávalos, J E García-Ortiz, D García-Cruz, et al.
Gynecologic and Obstetric Investigation|June 1, 2000
Reproductive history in mothers of children with neural tube defectsF Rivas, I P Dávalos, N Olivares, et al.
Annales De Genetique|January 5, 2002
Del Xq23 in a mosaic Turner female: molecular and cytogenetic studiesV M Mesa-Cornejo, D García-Cruz, N Monroy-Jaramillo, et al.
Genetic Counseling (Geneva, Switzerland)|May 3, 2003
A variant example of familial Floating-Harbor syndrome?J M Peñaloza, D García-Cruz, I P Dávalos, et al.
Annales De Genetique|February 13, 2001
Ring-20-syndrome and loss of telomeric regionsD García-Cruz, A I Vásquez, D Perez-Rulfo, et al.
The British Journal of Dermatology|November 26, 2005
A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalpN O Dávalos, A García-Vargas, J Pforr, et al.
Genetic Counseling (Geneva, Switzerland)|May 28, 2011
Wide clinical spectrum in Zimmermann-Laband syndromeI P Davalos, A J L Brambila-Tapia, N O Dávalos, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Clinical Dysmorphology|July 19, 2003
Myhre syndrome: first female caseN O Dávalos, J E García-Ortiz, D García-Cruz, et al.
Gynecologic and Obstetric Investigation|June 1, 2000
Reproductive history in mothers of children with neural tube defectsF Rivas, I P Dávalos, N Olivares, et al.
Annales De Genetique|January 5, 2002
Del Xq23 in a mosaic Turner female: molecular and cytogenetic studiesV M Mesa-Cornejo, D García-Cruz, N Monroy-Jaramillo, et al.
Genetic Counseling (Geneva, Switzerland)|May 3, 2003
A variant example of familial Floating-Harbor syndrome?J M Peñaloza, D García-Cruz, I P Dávalos, et al.
Annales De Genetique|February 13, 2001
Ring-20-syndrome and loss of telomeric regionsD García-Cruz, A I Vásquez, D Perez-Rulfo, et al.
The British Journal of Dermatology|November 26, 2005
A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalpN O Dávalos, A García-Vargas, J Pforr, et al.
Genetic Counseling (Geneva, Switzerland)|May 28, 2011
Wide clinical spectrum in Zimmermann-Laband syndromeI P Davalos, A J L Brambila-Tapia, N O Dávalos, et al.
Pageof 1