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Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST).
Hum Mol Genet. 2001 Mar 1;10(5):537-43. doi: 10.1093/hmg/10.5.537.
Hum Mol Genet. 2001.
PMID: 11181578
Autosomal recessive malformation syndrome with minor manifestation in the heterozygotes: a preliminary report of a possible new syndrome.
Paes-Alves AF, Azevêdo ES, Sousa MG, Almeida-Melo N, Oliveira-Filho OJ.
Paes-Alves AF, et al.
Am J Med Genet. 1991 Nov 1;41(2):141-52. doi: 10.1002/ajmg.1320410202.
Am J Med Genet. 1991.
PMID: 1785624
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Short stature in a patient with cystic fibrosis caused by a 6.7-kb human growth hormone gene deletion.
Mullis PE, Liechti-Gallati S, Di Silvio L, Brook CG, Paes-Alves AF.
Mullis PE, et al. Among authors: paes alves af.
Horm Res. 1991;36(1-2):4-8. doi: 10.1159/000182097.
Horm Res. 1991.
PMID: 1687684
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Anthropometric data of children heterozygous for abnormal hemoglobins (Hb AS, Hb AC) and paired controls Hb AA.
Freire-Maia N, Paes Alves AF, Oliveira MP, Olympio da Silva MC, Lima Machado MA, Azevêdo ES.
Freire-Maia N, et al. Among authors: paes alves af.
Hum Hered. 1981;31(2):70-3. doi: 10.1159/000153180.
Hum Hered. 1981.
PMID: 7228060
No abstract available.
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