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Results: 1-6 |
Results: 6

Authors: BELLONI E MUENKE M ROESSLER E TRAVERSO G SIEGELBARTELT J FRUMKIN A MITCHELL HF DONISKELLER H HELMS C HING AV HENG HHQ KOOP B MARTINDALE D ROMMENS JM TSUI LC SCHERER SW
Citation: E. Belloni et al., IDENTIFICATION OF SONIC HEDGEHOG AS A CANDIDATE GENE RESPONSIBLE FOR HOLOPROSENCEPHALY, Nature genetics, 14(3), 1996, pp. 353-356

Authors: SAWYER JR LUKACS JL HASSED SJ ARNOLD GL MITCHELL HF MUENKE M
Citation: Jr. Sawyer et al., SUBBAND DELETION OF 7Q36.3 IN A PATIENT WITH RING CHROMOSOME-7 - ASSOCIATION WITH HOLOPROSENCEPHALY, American journal of medical genetics, 65(2), 1996, pp. 113-116

Authors: ROBIN NH FELDMAN GJ ARONSON AL MITCHELL HF WEKSBERG R LEONARD CO BURTON BK JOSEPHSON KD LAXOVA R ALECK KA ALLANSON JE GUIONALMEIDA ML MARTIN RA LEICHTMAN LG PRICE RA OPITZ JM MUENKE M
Citation: Nh. Robin et al., OPITZ-SYNDROME IS GENETICALLY HETEROGENEOUS, WITH ONE LOCUS ON XP22, AND A 2ND LOCUS ON 22Q11.2, Nature genetics, 11(4), 1995, pp. 459-461

Authors: MUENKE M BONE LJ MITCHELL HF HART I WALTON K HALLJOHNSON K IPPEL EF DIETZBAND J KVALOY K FAN CM TESSIERLAVIGNE M PATTERSON D
Citation: M. Muenke et al., PHYSICAL MAPPING OF THE HOLOPROSENCEPHALY CRITICAL REGION IN 21Q22.3,EXCLUSION OF SIM2 AS A CANDIDATE GENE FOR HOLOPROSENCEPHALY, AND MAPPING OF SIM2 TO A REGION OF CHROMOSOME-21 IMPORTANT FOR DOWN-SYNDROME, American journal of human genetics, 57(5), 1995, pp. 1074-1079

Authors: OVERHAUSER J MITCHELL HF ZACKAI EH TICK DB ROJAS K MUENKE M
Citation: J. Overhauser et al., PHYSICAL MAPPING OF THE HOLOPROSENCEPHALY CRITICAL REGION IN 18P11.3, American journal of human genetics, 57(5), 1995, pp. 1080-1085

Authors: ROBIN NH FELDMAN GJ MITCHELL HF LORENZ P WILROY RS ZACKAI EH ALLANSON JE REICH EW PFEIFFER RA CLARKE LA WARMAN ML MULLIKEN JB BRUETON LA WINTER RM PRICE RA GASSER DL MUENKE M
Citation: Nh. Robin et al., LINKAGE OF PFEIFFER-SYNDROME TO CHROMOSOME-8 CENTROMERE AND EVIDENCE FOR GENETIC-HETEROGENEITY, Human molecular genetics, 3(12), 1994, pp. 2153-2158
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