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A Delicado Navarro

Showing results (1-10 of 8) with videos related to

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Genetic Counseling (Geneva, Switzerland)|November 5, 1999
Familial deletion of 22q11.2G Rodríguez Criado, J Gruesomontero, A Delicado Navarro
Acta Obstetrica Y Ginecologica Hispano-Lusitana|March 1, 1979
[Sterility and deletion of the fluorescent zone of the Y chromosome]E Barreiro, I López Pajares, A Delicado Navarro, et al.
Anales Espanoles De Pediatria|December 22, 1998
[Smith-Magenis syndrome: a case report]S Quijano Roy, A Delicado Navarro, I López Pajares, et al.
Anales Espanoles De Pediatria|March 1, 1993
[A case of neonatal Pallister-Killian syndrome (tetrasomy 12p)]J González de Dios, A García-Alix Pérez, A Díaz de Bustamante, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|June 23, 2004
[Williams-Beuren syndrome: presentation of 82 cases]I Pascual-Castroviejo, S I Pascual-Pascual, F Moreno Granado, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|March 11, 2006
[Clinical guide to the management of patients with Beckwith-Wiedemann syndrome]P Lapunzina Badía, M del Campo Casanelles, A Delicado Navarro, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|June 24, 2006
[Holt-Oram syndrome: characterization of a novel mutation]L Fernández García-Moya, P Lapunzina Badía, A Delicado Navarro, et al.
Journal of Medical Genetics|March 7, 2009
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotypeT Kleefstra, W A van Zelst-Stams, W M Nillesen, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
Familial deletion of 22q11.2G Rodríguez Criado, J Gruesomontero, A Delicado Navarro
Acta Obstetrica Y Ginecologica Hispano-Lusitana|March 1, 1979
[Sterility and deletion of the fluorescent zone of the Y chromosome]E Barreiro, I López Pajares, A Delicado Navarro, et al.
Anales Espanoles De Pediatria|December 22, 1998
[Smith-Magenis syndrome: a case report]S Quijano Roy, A Delicado Navarro, I López Pajares, et al.
Anales Espanoles De Pediatria|March 1, 1993
[A case of neonatal Pallister-Killian syndrome (tetrasomy 12p)]J González de Dios, A García-Alix Pérez, A Díaz de Bustamante, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|June 23, 2004
[Williams-Beuren syndrome: presentation of 82 cases]I Pascual-Castroviejo, S I Pascual-Pascual, F Moreno Granado, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|March 11, 2006
[Clinical guide to the management of patients with Beckwith-Wiedemann syndrome]P Lapunzina Badía, M del Campo Casanelles, A Delicado Navarro, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|June 24, 2006
[Holt-Oram syndrome: characterization of a novel mutation]L Fernández García-Moya, P Lapunzina Badía, A Delicado Navarro, et al.
Journal of Medical Genetics|March 7, 2009
Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotypeT Kleefstra, W A van Zelst-Stams, W M Nillesen, et al.
Pageof 1