AAAAAA

   
Results: 1-2 |
Results: 2

Authors: NANCE MA ABRAMSON R ASHIZAWA T CODORI AM FOX M GETTIG B MYERS RH QUAID K SELTZER W SHEA DK WEXLER N ZANKO A PROUD V RICHTER S HAUCK L BROOME D BASS H JONES OW ZANKO A BODELL A TAYLOR L HAVERKAMP C HEIMLER A DIMAIO M HAUN R DIAMOND T JONES R YIM D DONLON S EVERS C SHANNON K LEBEL R POLZIN S MILLER J QUAID K GRAY C GODFREY N MYERS R UHLMANN W LUDOWESE C LEROY B OTTO E JOHNSON J MCCORMACK M COPE J PALLADINO L LEWIS J MCKENNA C HICKEY C THOMSON L WATERSON J HUELSMAN K LINARD S SCHAEFER F RUBENSTEIN J KOVAK K GOODWIN D GODMILOW L SCHRAMKE C SKOREYSOLLBERG P POTTER N HANNIG V BROOKSHIRE G HELLER K KESTER M LEONARD K MENGDEN GA BATY B ALLINSON P BENNETT R HINER B GOONEWARDENA P SPECTOR E MCINTOSH N MUELLER OT SHOFFNER J BERRYKRAVIS E DEMARCHI J KASCH L MATTHIASHAGEN V BARTHOLOMEW D PRIOR T SCHAEFER F GOODWIN D VNENCAKJONES C POTTER N RICHARDS S
Citation: Ma. Nance et al., GENETIC TESTING OF CHILDREN AT RISK FOR HUNTINGTONS-DISEASE, Neurology, 49(4), 1997, pp. 1048-1053

Authors: JUYAL RC GREENBERG F MENGDEN GA LUPSKI JR TRASK BJ VANDENENGH G LINDSAY EA CHRISTY H CHEN KS BALDINI A SHAFFER LG PATEL PI
Citation: Rc. Juyal et al., SMITH-MAGENIS SYNDROME DELETION - A CASE WITH EQUIVOCAL CYTOGENETIC FINDINGS RESOLVED BY FLUORESCENCE IN-SITU HYBRIDIZATION, American journal of medical genetics, 58(3), 1995, pp. 286-291
Risultati: 1-2 |