Authors:
ZATZ M
MARIE SK
CERQUEIRA A
VAINZOF M
PAVANELLO RCM
PASSOSBUENO MR
Citation: M. Zatz et al., THE FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD1) GENE AFFECTS MALESMORE SEVERELY AND MORE FREQUENTLY THAN FEMALES, American journal of medical genetics, 77(2), 1998, pp. 155-161
Authors:
MINGRONINETTO RC
PAVANELLO RCM
OTTO PA
VIANNAMORGANTE AM
Citation: Rc. Mingroninetto et al., EXPERIENCE WITH MOLECULAR AND CYTOGENETIC DIAGNOSIS OF FRAGILE-X-SYNDROME IN BRAZILIAN FAMILIES, BRAZ J GENE, 20(4), 1997, pp. 731-739
Authors:
BONNEMANN CG
PASSOSBUENO MR
MCNALLY EM
VAINZOF M
MOREIRA ED
MARIE SK
PAVANELLO RCM
NOGUCHI S
OZAWA E
ZATZ M
KUNKEL LM
Citation: Cg. Bonnemann et al., GENOMIC SCREENING FOR BETA-SARCOGLYCAN GENE-MUTATIONS - MISSENSE MUTATIONS MAY CAUSE SEVERE LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2E (LGMD 2E), Human molecular genetics, 5(12), 1996, pp. 1953-1961
Authors:
VAINZOF M
PASSOSBUENO MR
CANOVAS M
MOREIRA ES
PAVANELLO RCM
MARIE SK
ANDERSON LVB
BONNEMANN CG
MCNALLY EM
NIGRO V
KUNKEL LM
ZATZ M
Citation: M. Vainzof et al., THE SARCOGLYCAN COMPLEX IN THE 6 AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHIES, Human molecular genetics, 5(12), 1996, pp. 1963-1969
Authors:
ZATZ M
PASSOSBUENO MR
CERQUEIRA A
MARIE SK
VAINZOF M
PAVANELLO RCM
Citation: M. Zatz et al., ANALYSIS OF THE CTG REPEAT IN SKELETAL-MUSCLE OF YOUNG AND ADULT MYOTONIC-DYSTROPHY PATIENTS - WHEN DOES THE EXPANSION OCCUR, Human molecular genetics, 4(3), 1995, pp. 401-406
Authors:
VAINZOF M
MARIE SKN
REED UC
SCHWARTZMAN JS
PAVANELLO RCM
PASSOSBUENO MR
ZATZ M
Citation: M. Vainzof et al., DEFICIENCY OF MEROSIN (LAMININ-M OR ALPHA-2) IN CONGENITAL MUSCULAR-DYSTROPHY ASSOCIATED WITH CEREBRAL WHITE-MATTER ALTERATIONS, Neuropediatrics, 26(6), 1995, pp. 293-297
Authors:
VAINZOF M
PASSOSBUENO MR
PAVANELLO RCM
ZATZ M
Citation: M. Vainzof et al., IS DYSTROPHIN ALWAYS ALTERED IN BECKER MUSCULAR-DYSTROPHY PATIENTS, Journal of the neurological sciences, 131(1), 1995, pp. 99-104
Authors:
ZATZ M
MATSUMURA K
VAINZOF M
PASSOSBUENO MR
PAVANELLO RCM
MARIE SK
CAMPBELL KP
Citation: M. Zatz et al., ASSESSMENT OF THE 50-KDA DYSTROPHIN-ASSOCIATED GLYCOPROTEIN IN BRAZILIAN PATIENTS WITH SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY, Journal of the neurological sciences, 123(1-2), 1994, pp. 122-128