Suchergebnisse - "Dobyns, William B"

PubPharm (6)

1

STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly

enthalten in: Human genetics | 2014

von Kakar, N. | Ahmad, J. | Morris-Rosendahl, D. | +7

2

STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly

enthalten in: Human genetics | 2014

von Kakar, N. | Ahmad, J. | Morris-Rosendahl, D. | +7

3

Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism

enthalten in: Human genetics | 2014

von Mirzaa, G. | Vitre, B. | Carpenter, G. | +6

4

Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism

enthalten in: Human genetics | 2014

von Mirzaa, G. | Vitre, B. | Carpenter, G. | +6

5

Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity

enthalten in: Human genetics | 2008

von Jalali, A. | Aldinger, K. | Chary, A. | +17

6

Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity

enthalten in: Human genetics | 2008

von Jalali, A. | Aldinger, K. | Chary, A. | +17

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