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Session 3 |
Date Sept 16 |
Chairman: Hans v Bokhoven |
Title Session ARMR - Mapping |
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Time |
Old abstract # |
New
abstract # |
Presenter |
Title
Presentation |
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11:40-
12:00 |
7 |
Wei
Chen |
Chromosome sorting and next generation sequencing in
consanguineous families with autosomal recessive mental retardation:
separating the wheat from the chaff |
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12:00
– 12:20 |
8 |
Hao Hu |
Homozygosity mapping in 4 unrelated Iranian families with autosomal
recessive mental retardation identifies overlapping linkage intervals on
chromosome REGION 1p34: a frequent cause of ARMR? |
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12:20
– 12:40 |
9 |
Lia Abbasi Moheb |
Two independent mutations in the ZNF526 gene cause
non-syndromic autosomal recessive mental retardation |
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12:40
– 13:00 |
10 |
Hossein Najmabadi |
HOMOZYGOSITY
MAPPING OF PRIMARY MICROCEPHALY IN 86 IRANIAN FAMILIES: NOVEL MUTATIONS AND
PHENOTYPES |
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13:00
– 13:20 |
11 |
Andreas
Tzschach |
A
NOVEL AUTOSOMAL RECESSIVE MR/MCA SYNDROME COMPRISING SHORT STATURE,
BRACHYDACTYLY AND PECTUS EXCAVATUM MAPS TO 5q23-q32 |
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13:00 – 13:40 |
12 |
Janneke Schuurs-Hoeijmakers |
GENES FOR AUTOSOMAL
RECESSIVE MENTAL RETARDATION IN OUTBRED FAMILIES |
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