Passalacqua, Cristóbal
9  Ergebnisse:
Personensuche X
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1

STAAR, a phase I/II study of isaralgagene civaparvovec (ST-..:

Hopkin, Robert J. ; Ganesh, Jaya ; Deegan, Patrick...
Molecular Genetics and Metabolism.  138 (2023)  2 - p. 107152 , 2023
 
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3

A novel MEFV gene mutation (A511V) in a Chilean FMF patient:

Akar, Nejat ; Öztürk, Ayşenur ; Arslan, Çiğdem...
Egyptian Journal of Medical Human Genetics.  12 (2011)  1 - p. 21-24 , 2011
 
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4

A pigmentary skin defect is a new finding in Marshall–Smith..:

Passalacqua, Cristóbal ; Melo, Camila ; Martín, Luz María...
American Journal of Medical Genetics Part A.  155 (2011)  8 - p. 2015-2017 , 2011
 
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5

Two sisters resembling Gorlin–Chaudhry–Moss syndrome:

Aravena, Teresa ; Passalacqua, Cristóbal ; Pizarro, Oscar.
American Journal of Medical Genetics Part A.  155 (2011)  10 - p. 2552-2555 , 2011
 
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6

Congenital anomalies of poor prognosis. Genetics Consensus ..:

Pardo Vargas, Rosa A ; Aracena, Mariana ; Aravena, Teresa...
Revista Chilena de Pediatria, Volumen 87, Issue 5, 2018, Pages 422-431.  , 2016
 
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7

Two sisters resembling Gorlin-Chaudhry-Moss syndrome:

Aravena, Teresa ; Passalacqua, Cristóbal ; Pizarro, Oscar.
American Journal of Medical Genetics, Part A, Volumen 155, Issue 10, 2018, Pages 2552-2555.  , 2011
 
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