TY  - GEN
AU  - Siegert,E
AU  - Beier,L
AU  - Gräbner,H
TI  - [Homozygotic Pelger-Huet anomaly]
SN  - 0023-1495
PY  - 1983///1008
KW  - Heart Septal Defects, Ventricular
KW  - etiology
KW  - Homozygote
KW  - Humans
KW  - Infant
KW  - Intellectual Disability
KW  - Male
KW  - Pelger-Huet Anomaly
KW  - complications
N1  - Publication Type: Case Reports; English Abstract; Journal Article
ER  -