Suchergebnisse - "Tariq, Muhammad"

PubPharm (2)

1

A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22–q11.2

enthalten in: Human genetics | 2007

von Hassan, M. | Chishti, M. | Jamal, S. | +2

2

A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22–q11.2

enthalten in: Human genetics | 2007

von Hassan, M. | Chishti, M. | Jamal, S. | +2

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