Results 21 to 30 of about 46 (43)

Reply to Hofmann et al. [PDF]

Am J Hum Genet, 1998
Mackey D, Oostra RJ, Rosenberg T, Nikoskelainen E, Poulton J, Barratt T, Bolhuis P, Norby S, Savontaus ML, Chan C, Howell N.   +10 more
europepmc   +1 more source

The -75A-->C substitution in the 5' UTR of the Wilson disease gene is a sequence polymorphism in the Mediterranean population. [PDF]

Am J Hum Genet, 1998
Loudianos G, Dessi V, Lovicu M, Angius A, Cao A, Pirastu M.   +5 more
europepmc   +1 more source

Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype. [PDF]

Am J Hum Genet, 1998
Gottlieb S, Driscoll DA, Punnett HH, Sellinger B, Emanuel BS, Budarf ML.   +5 more
europepmc   +1 more source

Reply to Burghes. [PDF]

Am J Hum Genet, 1998
MacKenzie AE.
europepmc   +1 more source

A subtle case of iron-deficiency anemia. [PDF]

Intern Emerg Med, 2011
Sellitto A, Romano C, Giunta R, Galizia G, Lucivero G.   +4 more
europepmc   +1 more source

Alterazioni della crescita conseguenti a patologie surrenaliche insorte in età pediatrica

L Endocrinologo, 2023
Andrea Isidori, Marianna Minnetti, Valentina Sada   +2 more
exaly  

Sindrome di Cushing in età pediatrica

L Endocrinologo, 2020
Marco Cappa, Cappa Marco
exaly  

Minerva Pediatrica, Turin

JAMA - Journal of the American Medical Association, 1966
exaly   +6 more sources

MAV cerebrali in età pediatrica

The Neuroradiology Journal, 1992
C Mazza, A Maschio, E Piovan
exaly