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Results: 1-7 |
Results: 7
Monsters, myths and syndromes depicted on stamps
Authors: Chodirker, BN Chudley, AE
Citation: Bn. Chodirker et Ae. Chudley, Monsters, myths and syndromes depicted on stamps, CLIN GENET, 59(4), 2001, pp. 244-247
Fetal hepatic haemangioendothelioma: a new association with elevated maternal serum alpha-fetoprotein
Authors: Mhanni, AA Chodirker, BN Evans, JA Menticouglou, S Wiseman, N MacDonald, N Chudley, AE
Citation: Aa. Mhanni et al., Fetal hepatic haemangioendothelioma: a new association with elevated maternal serum alpha-fetoprotein, PRENAT DIAG, 20(5), 2000, pp. 433-435
Severe acro-renal-uterine-mandibular syndrome
Authors: Evans, JA Phillips, S Reed, M Chodirker, BN
Citation: Ja. Evans et al., Severe acro-renal-uterine-mandibular syndrome, AM J MED G, 93(1), 2000, pp. 67-73
Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype
Authors: Prasad, C Prasad, AN Chodirker, BN Lee, C Dawson, AK Jocelyn, LJ Chudley, AE
Citation: C. Prasad et al., Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype, CLIN GENET, 57(2), 2000, pp. 103-109
Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer
Authors: Bapat, BV Madlensky, L Temple, LKF Hiruki, T Redston, M Baron, DL Xia, L Marcus, VA Soravia, C Mitri, A Shen, W Gryfe, R Berk, T Chodirker, BN Cohen, Z Gallinger, S
Citation: Bv. Bapat et al., Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer, HUM GENET, 104(2), 1999, pp. 167-176
Untitled
Authors: Chudley, AE Dawson, AJ Chodirker, BN Jocelyn, LJ
Citation: Ae. Chudley et al., Untitled, J DEV BEH P, 20(1), 1999, pp. 72-73
Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affectingclinical outcome
Authors: Wang, MS Schinzel, A Kotzot, D Balmer, D Casey, R Chodirker, BN Gyftodimou, J Petersen, MB Lopez-Rangel, E Robinson, WP
Citation: Ms. Wang et al., Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affectingclinical outcome, AM J MED G, 86(1), 1999, pp. 34-43
Risultati: 1-7 |