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Results: 1-25 | 26-29 |
Results: 26-29/29
A NEW VARIANT OF THE NIJMEGEN BREAKAGE SYNDROME WITH MULTIPLE NONSPECIFIC CHROMOSOMAL-ANOMALIES AND A PARTICULAR PHENOTYPE
Authors: VAZKEN M DERKALOUSTIAN MD KLEIJER W VEKEMANS M MAZER B ELLIOTT AM BOOTH A ABISH S EYDOUX P
Citation: M. Vazken et al., A NEW VARIANT OF THE NIJMEGEN BREAKAGE SYNDROME WITH MULTIPLE NONSPECIFIC CHROMOSOMAL-ANOMALIES AND A PARTICULAR PHENOTYPE, American journal of human genetics, 57(4), 1995, pp. 624-624
DE-NOVO DELETION OF 22Q11 IN 2 MALE SIBLINGS WITH DIFFERENT PHENOTYPES
Authors: EYDOUX P KASPRZAK L ELLIOTT AM SHEVELL M DERKALOUSTIAN VM
Citation: P. Eydoux et al., DE-NOVO DELETION OF 22Q11 IN 2 MALE SIBLINGS WITH DIFFERENT PHENOTYPES, American journal of human genetics, 57(4), 1995, pp. 630-630
HETEROGENEITY OF TRICHOTHIODYSTROPHY-NEUROCUTANEOUS SYNDROME
Authors: SASI R ROSENFELD B EYDOUX P TEEBI AS
Citation: R. Sasi et al., HETEROGENEITY OF TRICHOTHIODYSTROPHY-NEUROCUTANEOUS SYNDROME, American journal of human genetics, 57(4), 1995, pp. 1783-1783
ASSIGNMENT OF THE GENE FOR CYSTINURIA (SLC3A1) TO HUMAN-CHROMOSOME 2P21 BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: ZHANG XX ROZEN R HEDIGER MA GOODYER P EYDOUX P
Citation: Xx. Zhang et al., ASSIGNMENT OF THE GENE FOR CYSTINURIA (SLC3A1) TO HUMAN-CHROMOSOME 2P21 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Genomics, 24(2), 1994, pp. 413-414
Risultati: 1-25 | 26-29 |