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Results 1 - 10 of 32 for Collaborative
  1. OFD1 gene 
    ... Franco B; Oral-Facial-Digital Type I (OFDI) Collaborative Group. Mutational spectrum of the oral-facial-digital ... digital syndrome type 1: a French and Belgian collaborative study. J Med Genet. 2006 Jan;43(1): ...
    https://medlineplus.gov/genetics/gene/ofd1 - Genetics
  2. Oral-facial-digital syndrome 
    ... Franco B; Oral-Facial-Digital Type I (OFDI) Collaborative Group. Mutational spectrum of the oral-facial-digital ... digital syndrome type 1: a French and Belgian collaborative study. J Med Genet. 2006 Jan;43(1): ...
    https://medlineplus.gov/.../condition/oral-facial-digital-syndrome - Genetics
  3. Osteoporosis-pseudoglioma syndrome 
    ... Heeger S, Bartels CF, Schelling DK; Osteoporosis-Pseudoglioma Collaborative Group. Clinical and molecular findings in osteoporosis-pseudoglioma ... R, Olsen BR, Warman ML; Osteoporosis-Pseudoglioma Syndrome Collaborative Group. LDL receptor-related protein 5 (LRP5) affects ...
    https://medlineplus.gov/.../osteoporosis-pseudoglioma-syndrome - Genetics
  4. Emanuel syndrome 
    ... Iselius L. The 11q;22q translocation: a European collaborative analysis of 43 cases. Hum Genet. 1980;56( ... N, et al. The 11q;22q translocation: a collaborative study of 20 new cases and analysis of ...
    https://medlineplus.gov/genetics/condition/emanuel-syndrome - Genetics
  5. INS gene 
    ... DF, Philipson LH, Bell GI; Neonatal Diabetes International Collaborative Group; Hattersley AT, Ellard S. Insulin mutation screening ... AT, Philipson LH, Bell GI; Neonatal Diabetes International Collaborative Group. Insulin gene mutations as a cause of ...
    https://medlineplus.gov/genetics/gene/ins - Genetics
  6. LRP5 gene 
    ... Heeger S, Bartels CF, Schelling DK; Osteoporosis-Pseudoglioma Collaborative Group. Clinical and molecular findings in osteoporosis-pseudoglioma ... R, Olsen BR, Warman ML; Osteoporosis-Pseudoglioma Syndrome Collaborative Group. LDL receptor-related protein 5 (LRP5) affects ...
    https://medlineplus.gov/genetics/gene/lrp5 - Genetics
  7. Otopalatodigital syndrome type 2 
    ... Jones J, Wilkie AO; OPD-spectrum Disorders Clinical Collaborative Group. Localized mutations in the gene encoding the ...
    https://medlineplus.gov/.../otopalatodigital-syndrome-type-2 - Genetics
  8. Melnick-Needles syndrome 
    ... Jones J, Wilkie AO; OPD-spectrum Disorders Clinical Collaborative Group. Localized mutations in the gene encoding the ...
    https://medlineplus.gov/genetics/condition/melnick-needles-syndrome - Genetics
  9. PTPN11 gene 
    ... C, Baumann C, Verloes A, Cave H; French Collaborative Noonan Study Group. PTPN11 mutations in patients with ...
    https://medlineplus.gov/genetics/gene/ptpn11 - Genetics
  10. Müllerian aplasia and hyperandrogenism 
    ... primary amenorrhea and mullerian duct abnormalities: a French collaborative study. J Clin Endocrinol Metab. 2008 Mar;93( ...
    https://medlineplus.gov/.../mullerian-aplasia-and-hyperandrogenism - Genetics
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