Authors: AHLBOM BE YAQOOB M LARSSON A ILICKI A ANNEREN G WADELIUS C

Citation: Be. Ahlbom et al., GENETIC AND LINKAGE ANALYSIS OF FAMILIAL CONGENITAL HYPOTHYROIDISM - EXCLUSION OF LINKAGE TO THE TSH RECEPTOR GENE, Human genetics, 99(2), 1997, pp. 186-190

Authors: AHLBOM BE SIDENVALL R ANNEREN G

Citation: Be. Ahlbom et al., DELETION OF CHROMOSOME-21 IN A GIRL WITH CONGENITAL HYPOTHYROIDISM AND MILD MENTAL-RETARDATION, American journal of medical genetics, 64(3), 1996, pp. 501-505

Authors: AHLBOM BE GOETZ P KORENBERG JR PETTERSSON U SEEMANOVA E WADELIUS C ZECH L ANNEREN G

Citation: Be. Ahlbom et al., MOLECULAR ANALYSIS OF CHROMOSOME-21 IN A PATIENT WITH A PHENOTYPE OF DOWN-SYNDROME AND APPARENTLY NORMAL KARYOTYPE, American journal of medical genetics, 63(4), 1996, pp. 566-572

Authors: AHLBOM BE DAHL N ZETTERQVIST P ANNEREN G

Citation: Be. Ahlbom et al., NOONAN SYNDROME WITH CAFE-AU-LAIT SPOTS AND MULTIPLE LENTIGINES SYNDROME ARE NOT LINKED TO THE NEUROFIBROMATOSIS TYPE-1 LOCUS, Clinical genetics, 48(2), 1995, pp. 85-89