Results 201 to 210 of about 2,689 (218)

Terminal deletion of (1)(q42) in a newborn.

Annales de genetique, 1984
M R, Montero, A, Martinez, J L, Fayos, V, Alvarez   +3 more
openaire   +1 more source

A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41‐q42 deletion phenotype

American Journal of Medical Genetics, Part A, 2018
Chris Balak, Newell Belnap, Keri Ramsey   +2 more
exaly  

Two siblings with partial trisomy 1(q42.3-ter)

Brain and Development, 1993
Yasuo Sunaga
exaly  

Pseudoreticulocytosis in a case of myelodysplastic syndrome with translocation t(1;14) (q42;q32).

Seminars in hematology, 1995
C, de Pree, C, Cabrol, J L, Frossard, P, Beris   +3 more
openaire   +1 more source

Hot deformation behavior and constitutive relationship of Q420qE steel

Central South University, 2011
Qian-Qian Liu, Wang Li-Jun
exaly  

Pseudohypoaldosteronism (PHA; 1q31-q42, 17p11-q21, 12p13, 16p13-p12)

2008
openaire   +1 more source

Experimental investigation on fatigue performance of three typical welded joints of Q420qFNH weathering steel

Construction and Building Materials
Chuang Cui
exaly  

Pseudohypoaldosteronism (PHA; 1q31-q42, 17p11-q21, 12p13, 16p13-p12)

2012
openaire   +1 more source

Conserved Residues R420 and Q428 in a Cytoplasmic Loop of the Citrate/Malate Transporter CimH of Bacillus subtilis Are Accessible from the External Face of the Membrane

Biochemistry, 2003
Bastiaan P Krom, Juke S Lolkema
exaly  

Corrosion behavior and random corrosion morphology reconstruction of welded joints of Q420qFNH weathering steel in a marine environment

Materials and Design
Chuang Cui
exaly