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1.
Clinical features for diagnosis and management of patients with PRDM12 congenital insensitivity to pain.
J Med Genet
; 53(8): 533-5, 2016 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-26975306
2.
Variation in health visiting contacts for children in England: cross-sectional analysis of the 2-2½ year review using administrative data (Community Services Dataset, CSDS).
BMJ Open
; 12(2): e053884, 2022 02 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-35193912
3.
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1.
BMC Med Genet
; 12: 106, 2011 Aug 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-21827697
4.
Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect.
Eur J Hum Genet
; 14(4): 418-25, 2006 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-16493439
5.
The presence of multiple regions of homozygous deletion at the CSMD1 locus in oral squamous cell carcinoma question the role of CSMD1 in head and neck carcinogenesis.
Genes Chromosomes Cancer
; 37(2): 132-40, 2003 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-12696061
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