trisomy 20 syndrome

tri·so·my 20 syn·drome

a chromosomal disorder characterized by profound mental retardation, coarse facies, macrostomia and macroglossia, minor anomalies of the ears, pigmentary dysplasia of the skin, dorsal kyphoscoliosis, and other skeletal defects.

tri·so·my 20 syn·drome

(trīsō-mē sindrōm) Chromosomal disorder characterized by profound mental retardation, coarse facies, macrostomia and macroglossia, minor anomalies of the ears, pigmentary dysplasia of skin, dorsal kyphoscoliosis, and other skeletal defects.

单词	trisomy 20 syndrome
释义	trisomy 20 syndrome tri·so·my 20 syn·drome a chromosomal disorder characterized by profound mental retardation, coarse facies, macrostomia and macroglossia, minor anomalies of the ears, pigmentary dysplasia of the skin, dorsal kyphoscoliosis, and other skeletal defects. tri·so·my 20 syn·drome a chromosomal disorder characterized by profound mental retardation, coarse facies, macrostomia and macroglossia, minor anomalies of the ears, pigmentary dysplasia of the skin, dorsal kyphoscoliosis, and other skeletal defects. tri·so·my 20 syn·drome (trīsō-mē sindrōm) Chromosomal disorder characterized by profound mental retardation, coarse facies, macrostomia and macroglossia, minor anomalies of the ears, pigmentary dysplasia of skin, dorsal kyphoscoliosis, and other skeletal defects.
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