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Results: 1-7 |
Results: 7

Authors: WANDSTRAT AE LEANACOX J JENKINS L SCHWARTZ S
Citation: Ae. Wandstrat et al., MOLECULAR CYTOGENETIC EVIDENCE FOR A COMMON BREAKPOINT IN THE LARGESTINVERTED DUPLICATIONS OF CHROMOSOME-15, American journal of human genetics, 62(4), 1998, pp. 925-936

Authors: AMOSLANDGRAF JM JI Y WANDSTRAT AE DRISCOLL DJ SCHWARTZ S NICHOLLS RD
Citation: Jm. Amoslandgraf et al., RECOMBINATION BETWEEN LARGE, TRANSCRIPTIONALLY ACTIVE REPEATED ELEMENTS AT THE PROXIMAL AND DISTAL BREAKPOINTS IN PRADER-WILLI AND ANGELMAN-SYNDROMES, American journal of human genetics, 61(4), 1997, pp. 5-5

Authors: WANDSTRAT AE SCHWARTZ S
Citation: Ae. Wandstrat et S. Schwartz, ISOLATION OF INV DUP(15) IN SOMATIC-CELL HYBRIDS - REFINING THE MECHANISM OF FORMATION, American journal of human genetics, 61(4), 1997, pp. 22-22

Authors: SCHWARTZ S KUMAR A BECKER LA CROWE CA HAREN JM TSUCHIYA K WANDSTRAT AE WOLFF DJ
Citation: S. Schwartz et al., MOLECULAR AND CYTOGENETIC ANALYSIS OF DE-NOVO TERMINAL DELETIONS - IMPLICATIONS FOR MECHANISM OF FORMATION, American journal of human genetics, 61(4), 1997, pp. 27-27

Authors: NICHOLLS RD AMOSLANDGRAF J WANDSTRAT AE SCHWARTZ S CASSIDY SB JI Y DRISCOLL DJ GLENN CC SUN Y PALMER CG BUITING K HORSTHEMKE B SAITOH S
Citation: Rd. Nicholls et al., MECHANISMS INVOLVED IN PRADER-WILLI AND ANGELMAN SYNDROME (VOL 64, PG573, 1996), American journal of medical genetics, 66(2), 1996, pp. 244-244

Authors: NICHOLLS RD AMOSLANDGRAF J WANDSTRAT AE SCHWARTZ S CASSIDY SB JI Y DRISCOLL DJ
Citation: Rd. Nicholls et al., MECHANISMS INVOLVED IN PRADER-WILLI AND ANGELMAN SYNDROME, American journal of medical genetics, 64(4), 1996, pp. 1-1

Authors: WANDSTRAT AE LEANACOX J SCHWARTZ S
Citation: Ae. Wandstrat et al., MOLECULAR CHARACTERIZATION OF INVERTED DUPLICATIONS OF CHROMOSOME-15 - INSIGHT INTO MECHANISM OF FORMATION, American journal of human genetics, 57(4), 1995, pp. 168-168
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