Results
|
|
1.
|
|
|
|
2.
|
|
|
|
3.
|
|
|
|
4.
|
|
|
|
5.
|
The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1-13.2. [electronic resource] by
- Roberts, E
- Jackson, A P
- Carradice, A C
- Deeble, V J
- Mannan, J
- Rashid, Y
- Jafri, H
- McHale, D P
- Markham, A F
- Lench, N J
- Woods, C G
Producer: 20000120
In:
European journal of human genetics : EJHG vol. 7
Availability: No items available.
|
|
|
6.
|
Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter. [electronic resource] by
- Jackson, A P
- McHale, D P
- Campbell, D A
- Jafri, H
- Rashid, Y
- Mannan, J
- Karbani, G
- Corry, P
- Levene, M I
- Mueller, R F
- Markham, A F
- Lench, N J
- Woods, C G
Producer: 19981224
In:
American journal of human genetics vol. 63
Availability: No items available.
|
|
|
7.
|
A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22. [electronic resource] by
- Campbell, D A
- McHale, D P
- Brown, K A
- Moynihan, L M
- Houseman, M
- Karbani, G
- Parry, G
- Janjua, A H
- Newton, V
- al-Gazali, L
- Markham, A F
- Lench, N J
- Mueller, R F
Producer: 19980204
In:
Journal of medical genetics vol. 34
Availability: No items available.
|
|
|
8.
|
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. [electronic resource] by
- Curtis, A R
- Fey, C
- Morris, C M
- Bindoff, L A
- Ince, P G
- Chinnery, P F
- Coulthard, A
- Jackson, M J
- Jackson, A P
- McHale, D P
- Hay, D
- Barker, W A
- Markham, A F
- Bates, D
- Curtis, A
- Burn, J
Producer: 20010816
In:
Nature genetics vol. 28
Availability: No items available.
|