Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPWJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC

Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY (VOL 6, PG 17, 1997), Human molecular genetics, 6(4), 1997, pp. 650-650

Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC

Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY, Human molecular genetics, 6(1), 1997, pp. 17-26

Authors: SMEETS H LEMMINK H NILLESEN W VANDRUNEN A VANDENHEUVEL L MONNENS L SCHRODER C

Citation: H. Smeets et al., TYPE-IV COLLAGEN DEFECTS IN ALPORT SYNDROME AND FAMILIAL BENIGN HEMATURIA, Kidney international, 50(1), 1996, pp. 330-330

Authors: LEMMINK HH VANDENHEUVEL L SCHRODER CAH NILLESEN W VANOOST BA BRUNNER HG MONNENS LAH SMEETS HJM

Citation: Hh. Lemmink et al., MOLECULAR AND IMMUNOLOGICAL STUDIES IN X-LINKED AND AUTOSOMAL RECESSIVE ALPORT SYNDROME, Journal of the American Society of Nephrology, 5(3), 1994, pp. 629-629

Authors: JANSEN G WILLEMS P COERWINKEL M NILLESEN W SMEETS H VITS L HOWELER C BRUNNER H WIERINGA B

Citation: G. Jansen et al., GONOSOMAL MOSAICISM IN MYOTONIC-DYSTROPHY PATIENTS - INVOLVEMENT OF MITOTIC EVENTS IN (CTG)(N) REPEAT VARIATION AND SELECTION AGAINST EXTREME EXPANSION IN SPERM, American journal of human genetics, 54(4), 1994, pp. 575-585

Authors: BRUNNER HG BRUGGENWIRTH HT NILLESEN W JANSEN G HAMEL BCJ HOPPE RLE DEDIE CEM HOWELER CJ VANOOST BA WIERINGA B ROPERS HH SMEETS HJM

Citation: Hg. Brunner et al., INFLUENCE OF SEX OF THE TRANSMITTING PARENT AS WELL AS OF PARENTAL ALLELE SIZE ON THE CTG EXPANSION IN MYOTONIC-DYSTROPHY (DM), American journal of human genetics, 53(5), 1993, pp. 1016-1023