Suchergebnisse - "Tariq, Muhammad"

PubPharm (10)

1

A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss

enthalten in: Human genetics | 2021

von Ullah, F. | Rauf, W. | Khan, K. | +12

2

A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss

enthalten in: Human genetics | 2021

von Ullah, F. | Rauf, W. | Khan, K. | +12

3

Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3

enthalten in: Human genetics | 2009

von Tariq, M. | Khan, M. | Ahmad, W.

4

Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3

enthalten in: Human genetics | 2009

von Tariq, M. | Khan, M. | Ahmad, W.

5

Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)

enthalten in: Human genetics | 2008

von Azeem, Z. | Jelani, M. | Naz, G. | +10

6

Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)

enthalten in: Human genetics | 2008

von Azeem, Z. | Jelani, M. | Naz, G. | +10

7

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

8

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

9

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3

enthalten in: Human genetics | 2006

von Khan, S. | Riazuddin, S. | Tariq, M. | +8

10

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3

enthalten in: Human genetics | 2006

von Khan, S. | Riazuddin, S. | Tariq, M. | +8

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