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Results: 1-5 |
Results: 5

Authors: HUQ AHMM SUTCLIFFE JS NAKAO M SHEN Y GIBBS RA BEAUDET AL
Citation: Ahmm. Huq et al., SEQUENCING AND FUNCTIONAL-ANALYSIS OF THE SNRPN PROMOTER - IN-VITRO METHYLATION ABOLISHES PROMOTER ACTIVITY, PCR methods and applications, 7(6), 1997, pp. 642-648

Authors: HUQ AHMM LOVELL RS OU CN BEAUDET AL CRAIGEN WJ
Citation: Ahmm. Huq et al., X-LINKED GLYCEROL KINASE-DEFICIENCY IN THE MOUSE LEADS TO GROWTH-RETARDATION, ALTERED FAT-METABOLISM, AUTONOMOUS GLUCOCORTICOID SECRETION AND NEONATAL DEATH, Human molecular genetics, 6(11), 1997, pp. 1803-1809

Authors: HUQ AHMM BRAVERMAN RM GREENBERG F BACINO CA RIMOIN DL LACHMAN RS LEVIN ML
Citation: Ahmm. Huq et al., THE POINTER SYNDROME - A NEW SYNDROME WITH SKELETAL ABNORMALITIES, CAMPTODACTYLY, FACIAL ANOMALIES, AND FEEDING DIFFICULTIES, American journal of medical genetics, 68(2), 1997, pp. 225-230

Authors: HUQ AHMM LOVELL RS SAMPSON MJ DECKER WK DINULOS MB DISTECHE CM CRAIGEN WJ
Citation: Ahmm. Huq et al., ISOLATION, MAPPING, AND FUNCTIONAL EXPRESSION OF THE MOUSE X-CHROMOSOME GLYCEROL KINASE GENE, Genomics, 36(3), 1996, pp. 530-534

Authors: HUQ AHMM GREENBERG F BACINO CA LEVIN ML
Citation: Ahmm. Huq et al., NEW SKELETAL DYSPLASIA SYNDROME WITH PROGRESSIVE BONE CHANGES, CAMPTODACTYLY, DYSMORPHIC FACIAL FEATURES, AND FEEDING DIFFICULTIES, American journal of human genetics, 57(4), 1995, pp. 508-508
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