Detalhe da pesquisa
1.
Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.
Mol Psychiatry
; 23(4): 973-984, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28397838
2.
Charge transport mechanisms of PbSnSe2 and observation of transition from direct to Fowler-Nordheim tunneling.
RSC Adv
; 14(9): 5812-5816, 2024 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38362072
3.
Spontaneous posterior rectus sheath hernia: A case report and literature review.
Int J Surg Case Rep
; 102: 107834, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36535177
4.
Solution combustion synthesis: the relevant metrics for producing advanced and nanostructured photocatalysts.
Nanoscale
; 14(33): 11806-11868, 2022 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35920714
5.
Sustainable chemical processing of flowing wastewater through microwave energy.
Chemosphere
; 287(Pt 1): 132035, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34474383
6.
Gallbladder lymphangioma simulating liver hydatid cyst: A case report.
Int J Surg Case Rep
; 98: 107540, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36037641
7.
Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from Pakistan.
Clin Genet
; 78(5): 478-83, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20345473
8.
Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan.
Clin Genet
; 87(3): 296-8, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25080166
9.
Study of electric conduction mechanisms in bismuth silicate nanofibers.
Sci Rep
; 10(1): 2775, 2020 Feb 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32066818
10.
Development of High-Performance Bismuth Sulfide Nanobelts Humidity Sensor and Effect of Humid Environment on its Transport Properties.
ACS Omega
; 4(1): 2030-2039, 2019 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-31459454
11.
Aposthia: a birth defect or normal quantitative recessive human genetic trait?
East Mediterr Health J
; 13(2): 280-6, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17684849
12.
Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.
Am J Med Genet
; 100(1): 62-5, 2001 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-11337751
13.
Investigation of change in surface area and grain size of cadmium titanate nanofibers upon annealing and their effect on oxygen sensing.
ACS Appl Mater Interfaces
; 6(6): 4542-9, 2014 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24564767
14.
Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1-17q25.3.
Clin Genet
; 66(1): 73-8, 2004 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15200512
15.
A novel missense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a consanguineous Pakistani family.
Br J Dermatol
; 158(3): 621-3, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18070203
16.
Milk-alkali syndrome: a reverberation of the past.
Singapore Med J
; 48(4): 359-60, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17384887
17.
Aposthia: a birth defect or normal quantitative recessive human genetic trait?
(East. Mediterr. health j).
em Inglês
| WHOLIS | ID: who-117250