Pages that link to "Q69446374"
Jump to navigation
Jump to search
The following pages link to Inheritance and phenotypic expression of a t(7;9)(q36;q34)mat (Q69446374):
Displaying 7 items.
- De novo 7q36 deletion: breakpoint analysis and types of holoprosencephaly. (Q32133736) (← links)
- Partial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15) (Q33674207) (← links)
- Cytogenetic findings indicate heterogeneity in patients with blepharophimosis, epicanthus inversus, and developmental delay (Q33675470) (← links)
- Double partial trisomy 9q34.1-->qter and 21pter-->q22.11: FISH and clinical findings (Q33679774) (← links)
- Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qter (Q40823400) (← links)
- Physical mapping of the holoprosencephaly critical region on chromosome 7q36. (Q41567717) (← links)
- Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly (Q48058539) (← links)