Search details
1.
Author Correction: Crowther et al. reply.
Nature
; 560(7716): E1, 2018 08.
Article
in English
| MEDLINE | ID: mdl-29875404
2.
Quantifying global soil carbon losses in response to warming.
Nature
; 540(7631): 104-108, 2016 11 30.
Article
in English
| MEDLINE | ID: mdl-27905442
3.
Crowther et al. reply.
Nature
; 554(7693): E7-E8, 2018 02 21.
Article
in English
| MEDLINE | ID: mdl-29469091
4.
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome.
Nat Genet
; 14(4): 392-9, 1996 Dec.
Article
in English
| MEDLINE | ID: mdl-8944018
5.
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome.
Nat Genet
; 13(4): 492-4, 1996 Aug.
Article
in English
| MEDLINE | ID: mdl-8696350
6.
Bone resorption in syndromes of the Ras/MAPK pathway.
Clin Genet
; 80(6): 566-73, 2011 Dec.
Article
in English
| MEDLINE | ID: mdl-21204800
7.
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
J Med Genet
; 46(6): 389-98, 2009 Jun.
Article
in English
| MEDLINE | ID: mdl-19346217
8.
Environmental stimulation reduces learning deficits in experimental cretinism.
Science
; 191(4227): 578-9, 1976 Feb 13.
Article
in English
| MEDLINE | ID: mdl-943127
9.
Contrasting decadal-scale changes in elevation and vegetation in two Long Island Sound salt marshes.
Estuaries Coast
; 40(3): 651-661, 2017 May 01.
Article
in English
| MEDLINE | ID: mdl-30008626
10.
Anthropocene survival of southern New England's salt marshes.
Estuaries Coast
; 40(3): 617-625, 2017 May 01.
Article
in English
| MEDLINE | ID: mdl-30271312
11.
Case-control study of the muscular compartments and osseous strength in neurofibromatosis type 1 using peripheral quantitative computed tomography.
J Musculoskelet Neuronal Interact
; 5(2): 145-9, 2005 Jun.
Article
in English
| MEDLINE | ID: mdl-15951630
12.
Di George anomaly and velocardiofacial syndrome.
Pediatrics
; 85(4): 526-30, 1990 Apr.
Article
in English
| MEDLINE | ID: mdl-2314965
13.
Marshall-Smith syndrome: two case reports and a review of pulmonary manifestations.
Pediatrics
; 71(2): 219-23, 1983 Feb.
Article
in English
| MEDLINE | ID: mdl-6823423
14.
Further delineation of the 10p deletion syndrome.
Pediatrics
; 73(5): 670-5, 1984 May.
Article
in English
| MEDLINE | ID: mdl-6718125
15.
Natural history of Wolf-Hirschhorn syndrome: experience with 15 cases.
Pediatrics
; 103(4 Pt 1): 830-6, 1999 Apr.
Article
in English
| MEDLINE | ID: mdl-10103318
16.
Survival in trisomy 18.
Am J Med Genet
; 49(2): 170-4, 1994 Jan 15.
Article
in English
| MEDLINE | ID: mdl-8116664
17.
Corpus callosum agenesis, facial anomalies, Robin sequence, and other anomalies: a new autosomal recessive syndrome?
Am J Med Genet
; 31(1): 17-23, 1988 Sep.
Article
in English
| MEDLINE | ID: mdl-3223497
18.
Neurofibromatosis type 1: A model condition for the study of the molecular basis of variable expressivity in human disorders.
Am J Med Genet
; 89(1): 7-13, 1999 Mar 26.
Article
in English
| MEDLINE | ID: mdl-10469431
19.
Health supervision and anticipatory guidance of individuals with Wolf-Hirschhorn syndrome.
Am J Med Genet
; 89(2): 111-5, 1999 Jun 25.
Article
in English
| MEDLINE | ID: mdl-10559766
20.
Umbilical cord agenesis in limb body wall defect.
Am J Med Genet
; 71(1): 97-105, 1997 Jul 11.
Article
in English
| MEDLINE | ID: mdl-9215777