R D Milner
Overview
Explore the profile of R D Milner including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
210
Citations
1381
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Milner R, Ross J, Froud D
Arch Dis Child
. 2010 Oct;
47(254):674.
PMID: 21032483
No abstract available.
2.
Milner R, Fekete M, Assan R, Hodge J
Arch Dis Child
. 2010 Oct;
47(251):152.
PMID: 21032469
No abstract available.
3.
Pernasetti F, Milner R, al Ashwal A, de Zegher F, Chavez V, Muller M, et al.
J Clin Endocrinol Metab
. 1998 Jun;
83(6):2079-83.
PMID: 9626142
Pit-1, a member of the POU-homeo domain protein family, is one of the transcription factors responsible for anterior pituitary development and pituitary-specific gene expression. Here, we describe seven children with...
4.
5.
Gibson R, Morgan N, Goldstein L, Pearson I, Kesterton I, Foot N, et al.
Hum Mutat
. 1996 Jan;
8(2):140-8.
PMID: 8844212
Fanconi anemia (FA) is an autosomal recessive disorder associated with hypersensitivity to DNA cross-linking agents and bone marrow failure. At least four complementation groups have been defined, and the FA...
6.
Cogan J, Phillips 3rd J, Schenkman S, Milner R, Sakati N
J Clin Endocrinol Metab
. 1994 Nov;
79(5):1261-5.
PMID: 7962317
Two families with familial isolated GH deficiency (IGHD) were studied, type II (autosomal dominant) and type I (autosomal recessive), whose GH1 genes exhibit cosegregation with IGHD. DNA sequencing of the...
7.
Gibson R, Ford D, Jansen S, Savoia A, Havenga C, Milner R, et al.
J Med Genet
. 1994 Nov;
31(11):868-71.
PMID: 7853372
Fanconi anaemia is an autosomal recessive disorder associated with increased chromosome breakage and progressive bone marrow failure. The gene for complementation group C (FACC) has been cloned and mapped to...
8.
Berg M, Peoples R, Perez-Jurado L, Guevara-Aguirre J, Rosenbloom A, Laron Z, et al.
Acta Paediatr Suppl
. 1994 Apr;
399:112-4.
PMID: 7949594
Eight different mutations were detected in the growth hormone (GH) receptor gene of patients with inherited GH receptor deficiency (GHRD; Laron syndrome) from five continents. All the mutations are located...
9.
Cogan J, Phillips 3rd J, Sakati N, Frisch H, Schober E, Milner R
J Clin Endocrinol Metab
. 1993 May;
76(5):1224-8.
PMID: 8496314
The GH1 genes of probands of two families with familial isolated GH deficiency (IGHD) were sequenced. Double stranded sequencing of the polymerase chain reaction (PCR) amplification products from genomic DNA...
10.
Milner R, Khallouf K, Gibson R, Hajianpour A, Mathew C
Arch Dis Child
. 1993 Jan;
68(1):101-3.
PMID: 8434992
A family in which three siblings born to related parents all manifested clinical abnormalities characteristic of Fanconi's anaemia (microcephaly, short stature, slow growth, beak nose, micrognathia, skin dyspigmentation and forearm...