Authors: KARIM MA NAGLE DL KANDIL HH BURGER J MOORE KJ SPRITZ RA

Citation: Ma. Karim et al., MUTATIONS IN THE CHEDIAK-HIGASHI-SYNDROME GENE (CHS1) INDICATE REQUIREMENT FOR THE COMPLETE 3801-AMINO-ACID CHS PROTEIN, Human molecular genetics, 6(7), 1997, pp. 1087-1089

Authors: KANDIL HH ALGHANEM MM SARWAT MA ALTHALLAB FS

Citation: Hh. Kandil et al., HENNA (LAWSONIA-INERMIS LINN) INDUCING HEMOLYSIS AMONG G6PD-DEFICIENTNEWBORNS - A NEW CLINICAL OBSERVATION, Annals of tropical paediatrics, 16(4), 1996, pp. 287-291

Authors: FUKAI K OH J KARIM MA MOORE KJ KANDIL HH ITO H BURGER J SPRITZ RA

Citation: K. Fukai et al., HOMOZYGOSITY MAPPING OF THE GENE FOR CHEDIAK-HIGASHI-SYNDROME TO CHROMOSOME 1Q42-Q44 IN A SEGMENT OF CONSERVED SYNTENY THAT INCLUDES THE MOUSE BEIGE LOCUS (BG), American journal of human genetics, 59(3), 1996, pp. 620-624

Authors: KANDIL HH GHULAM AS THALLAB FS ALGHANIM MM FARAG TI

Citation: Hh. Kandil et al., AUTOSOMAL RECESSIVE COMMON VARIABLE IMMUNODEFICIENCY REPORTS OF 7 RELATED-CHILDREN IN A BEDOUIN KINDRED, American journal of human genetics, 57(4), 1995, pp. 511-511

Authors: ALGHANIM MM KANDIL HH ABUTALEB MA FARAG TI

Citation: Mm. Alghanim et al., PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS, American journal of human genetics, 57(4), 1995, pp. 1768-1768

Authors: KANDIL HH ALGHANEM MM SARWAT MA ALNABI HMH ALAWAI SA FARAG TI

Citation: Hh. Kandil et al., CHEDIAK-HIGASHI-SYNDROME AMONG BEDOUINS, American journal of human genetics, 53(3), 1993, pp. 460-460