Normal view MARC view ISBD view

Developing a predictive understanding of landscape importance to the Punan-Pelancau of East Kalimantan, Borneo. [electronic resource]

By:

Cunliffe, Robert N

Contributor(s):

Producer: 20080226Description: 593-9 p. digitalISSN:

0044-7447

Subject(s):

Online resources:

Available from publisher's website

In: Ambio vol. 36

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

No physical items for this record

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

There are no comments on this title.

to post a comment.

Back to results

1 Aortic and pulmonary artery dilatation in Cantu syndrome: expanding the phenotype.
by Chew, Yi-Rong
2 Microcephaly with a simplified gyral pattern in a child with a de novo TUBA1A variant.
by Wei, Heming
3 TFAP2A mutation in a child and mother with predominantly ocular anomalies: non-classical presentation of branchio-oculo-facial syndrome.
by Si-Min Ng, Pamela
4 A novel Ser40Trp variant in IFITM5 in a family with osteogenesis imperfecta and review of the literature.
by Lim, Jiin Ying
5 Chromosome 12q24.31 microdeletion and congenital heart disease: a case report and review of the literature.
by Bhatia, Neha S
6 DICER1 deletion and 14q32 microdeletion syndrome: an additional case and a review of the literature.
by Ting, Teck Wah
7 Left Ventricular Non-compaction: Is It Genetic?
by Ting, Teck Wah
8 Further delineation of CDC45-related Meier-Gorlin syndrome with craniosynostosis and review of literature.
by Ting, Chun Yi
9 Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine?
by Jamuar, Saumya Shekhar
10 Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome.
by Bonnard, Carine
11 A Report on Ten Asia Pacific Countries on Current Status and Future Directions of the Genetic Counseling Profession: The Establishment of the Professional Society of Genetic Counselors in Asia.
by Laurino, Mercy Y
12 De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations.
by Reijnders, Margot R F
13 Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.
by Hengel, Holger