the previously known genes contained in the genomic clones have been isolated. In addition, . et al. 0 we have isolated human genes that have already been described but not assigned to any chromosomal region.;1995-09;07/03/2016 15:25;07/03/2016 15:25;;617-622;;9;6;;Mamm. Genome;;;;;;;;eng;;;;;PubMed;;PMID: 8535069 - issue: - volume: - pages: .
and brain fog (48%). Severe limitations in daily life were reported in 31% of patients. Most PPCC care programs organized in-person visits with multidisciplinary teams. Diagnostic testing for respiratory and cardiac morbidity was most frequently performed and seldom abnormal. Treatment was often limited to physical therapy and psychological support. CONCLUSIONS: We found substantial heterogeneity in both the diagnostics and management of PPCC, . et al. 0 possibly explained by scarce scientific evidence and lack of standardized care. We present a list of components which future guidelines should address - issue: - volume: - pages: .
remarkably good agreement was found between the two sources of information. Digit preference was present to a limited degree. There were no important differences between the two questionnaire versions. At the individual level, . et al. 0 some misclassification was evident. For the detection of clinical infertility - issue: - volume: - pages: .
A l c a r a z G, . et al. 0 M i c h o n F X M i g n o t C L e s c a G - issue: T r a u f f l e r A - volume: B a d e n s C - pages: D e L a V a i s s i .
L., . et al. 0 D. R.";Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome).;Cell;;0092-8674;10.1016/0092-8674(95)90287-2;;The ATR-X syndrome is an X-linked disorder comprising severe psychomotor retardation RAD54 - issue: indicating that it could be a global transcriptional regulator. In addition to its role in the ATR-X syndrome - volume: XH2 m - pages: down-regulates expression of several genes.
under exclusive licence to the International Pediatric Research Foundation, . et al. 0 Inc.;;;;;;Place: United States PMID: 38287106 - issue: - volume: - pages: .
OCs have been on the market for 30 years and widely used for 20 years. Trends in other known risk factors for endometrial cancer would tend to have increased its incidence in that time in women under 55 years of age. Vital statistics however show a decrease for endometrial cancer mortality (41%) and morbidity (15%) in that group. This suggests an important protective effect of OCs on this disease., . et al. 0 - issue: - volume: - pages: .
called TBX22, . et al. 0 is composed of seven exons spanning 8.7 kilobases of genomic DNA in Xq21.1. The TBX22 mRNA is 2099 base pairs long and encodes a 400-amino-acids protein containing a T-domain in its NH(2)-terminal region which has the unique fea - issue: - volume: - pages: .
Florence, . et al. 0 Pierre; Desnous Florence";Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability.;Human molecular genetics;;1460-2083 0964-6906;10.1093/hmg/ddad203;;Intellectual... - issue: - volume: - pages: .
L.", . et al. 0 England);;0140-6736;10.1016/s0140-6736(89)92826-2;;;17/06/1989;04/08/2025 08:04;04/08/2025 08:04;;1385-1386;;8651;1;;Lancet;;;;;;;;eng;;;;;;;Place: England PMID: 2567394 - issue: - volume: - pages: .
M. P.", . et al. 0 England);;0140-6736;10.1016/s0140-6736(89)91743-1;;;18/02/1989;04/08/2025 08:04;04/08/2025 08:04;;377;;8634;1;;Lancet;;;;;;;;eng;;;;;;;Place: England PMID: 2563521 - issue: - volume: - pages: .