Guízar Vázquez J, Arredondo Vega F, Navarrete Cadena C, Cortés Chávez R
Bol Med Hosp Infant Mex. 1978 Nov-Dec;35(6):1155-60.
The present paper describes a family with daughter and son affected with clinical characteristics of Pierre Robin's anomaly. The pedigree suggests an autosomal recessive inheritance pattern. The authors mention that in order to have more genetic evidence on this trait, an extensive study of families, with at least one proband should be made for a correct genetic analysis.
本文描述了一个有女儿和儿子受皮埃尔·罗宾异常临床特征影响的家庭。系谱显示为常染色体隐性遗传模式。作者提到，为了获得关于该特征的更多遗传证据，应该对至少有一个先证者的家庭进行广泛研究，以便进行正确的遗传分析。
