Normal view MARC view ISBD view

Prenatal Cushing's syndrome secondary to nodular adrenocortical hyperplasia with unsuppressed plasma ACTH levels. [electronic resource]

By:

Tillmann, V

Contributor(s):

Producer: 20060328Description: 1127-31 p. digitalISSN:

0334-018X

Subject(s):

Online resources:

Available from publisher's website

In: Journal of pediatric endocrinology & metabolism : JPEM vol. 18

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: Case Reports; Journal Article

There are no comments on this title.

to post a comment.

Previous

Back to results

Next

1
2
3
4
5
6
7
8
9
10

1 Diamond Blackfan anaemia in the UK: clinical and genetic heterogeneity.
by Orfali, Karen A
2 Two-phase culture in Diamond Blackfan anemia: localization of erythroid defect.
by Ohene-Abuakwa, Yaw
3 Oxygen dependence of K(+)-Cl- cotransport in human red cell ghosts and sickle cells.
by Khan, Asif I
4 Islands within an island: Population genetic structure of the endemic Sardinian newt,
by Ball, Sarah E
5 Favorable effect on acute and chronic graft-versus-host disease with cyclophosphamide and in vivo anti-CD52 monoclonal antibodies for marrow transplantation from HLA-identical sibling donors for acquired aplastic anemia.
by Gupta, Vikas
6 Guidelines for the diagnosis and management of aplastic anaemia.
by Marsh, Judith C W
7 Ribosomal protein genes RPS10 and RPS26 are commonly mutated in Diamond-Blackfan anemia.
by Doherty, Leana
8 Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patients.
by Gazda, Hanna T
9 Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia.
by Farrar, Jason E
10 Ribosomal protein S24 gene is mutated in Diamond-Blackfan anemia.
by Gazda, Hanna T

Close