Molecular genetics of holoprosencephaly

scientific article

Molecular genetics of holoprosencephaly is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

External links are
P356DOI10.2741/NANNI
P8608Fatcat IDrelease_hszaqrt3zfha7og6lr4fgr3nje
P698PubMed publication ID10704430

P2093author name stringNanni L
Muenke MT
Schelper RL
P921main subjectholoprosencephalyQ1459821
P304page(s)D334-42
P577publication date2000-03-01
P1433published inFrontiers in BioscienceQ5506062
P1476titleMolecular genetics of holoprosencephaly
P478volume5

Reverse relations

cites work (P2860)
Q56261843Alobar holoprosencephaly associated with a rare chromosomal abnormality: Case report and literature review
Q50267594Cyclopia: isolated and with agnathia-otocephaly complex
Q38641243Facial Morphogenesis: Physical and Molecular Interactions Between the Brain and the Face.
Q48156828Genetically induced abnormal cranial development in human trisomy 18 with holoprosencephaly: comparisons with the normal tempo of osteogenic-neural development
Q21203684Histogenesis of retinal dysplasia in trisomy 13
Q36930083Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype
Q40627782Partial deletions of the long arm of chromosome 13 associated with holoprosencephaly and the Dandy-Walker malformation
Q37109640Semilobar Holoprosencephaly with Neurogenic Hypernatraemia: Two new cases

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