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Results: 1-8 |
Results: 8

Authors: PELLEGRINO JE LENSCH MW MUENKE M CHANCE PF
Citation: Je. Pellegrino et al., CLINICAL AND MOLECULAR ANALYSIS IN JOUBERT-SYNDROME, American journal of medical genetics, 72(1), 1997, pp. 59-62

Authors: GRAF WD CHANCE PF LENSCH MW ENG LJ LIPE HP THOMAS TD
Citation: Wd. Graf et al., SEVERE VINCRISTINE NEUROPATHY IN CHARCOT-MARIE-TOOTH-DISEASE TYPE-1A, Cancer, 77(7), 1996, pp. 1356-1362

Authors: KIYOSAWA H LENSCH MW CHANCE PF
Citation: H. Kiyosawa et al., ANALYSIS OF THE CMT1A-REP REPEAT - MAPPING CROSSOVER BREAKPOINTS IN CMT1A AND HNPP, Human molecular genetics, 4(12), 1995, pp. 2327-2334

Authors: BONE LJ DAHL N LENSCH MW CHANCE PF KELLY T LEGUERN E MAGI S PARRY G SHAPIRO H WANG S FISCHBECK KH
Citation: Lj. Bone et al., NEW CONNEXIN32 MUTATIONS ASSOCIATED WITH X-LINKED CHARCOT-MARIE-TOOTHDISEASE, Neurology, 45(10), 1995, pp. 1863-1866

Authors: CHANCE PF ABBAS N LENSCH MW PENTAO L ROA BB PATEL PI LUPSKI JR
Citation: Pf. Chance et al., 2 AUTOSOMAL-DOMINANT NEUROPATHIES RESULT FROM RECIPROCAL DNA DUPLICATION DELETION OF A REGION ON CHROMOSOME-17/, Human molecular genetics, 3(2), 1994, pp. 223-228

Authors: CHANCE PF LENSCH MW LIPE H BROWN RH BROWN RH BIRD TD
Citation: Pf. Chance et al., HEREDITARY NEURALGIC AMYOTROPHY AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - 2 DISTINCT GENETIC-DISORDERS, Neurology, 44(12), 1994, pp. 2253-2257

Authors: BERGOFFEN J SCHERER SS WANG S SCOTT MO BONE LJ PAUL DL CHEN K LENSCH MW CHANCE PF FISCHBECK KH
Citation: J. Bergoffen et al., CONNEXIN MUTATIONS IN X-LINKED CHARCOT-MARIE-TOOTH DISEASE, Science, 262(5142), 1993, pp. 2039-2042

Authors: ABBAS N LENSCH MW PENTAO L SMITH B MATSUNAMI N ROA B PATEL P CHANCE P LUPSKI JR
Citation: N. Abbas et al., 2 HUMAN PERIPHERAL NEUROPATHIES RESULT FROM RECIPROCAL UNEQUAL CROSSOVER, American journal of human genetics, 53(3), 1993, pp. 15-15
Risultati: 1-8 |