Amelia: A multi-center descriptive epidemiologic study in a large dataset from the International Clearinghouse for Birth Defects Surveillance and Research, and overview of the literature

A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra-amelia in two Saudi families

(2011) Wafaa Eyaid et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Very rare defects: What can we learn?

(2011) Eduardo E. Castilla et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Tubular jejunal duplication, amelia and congenital diaphragmatic eventration in a neonate

(2010) Chen-Yin Lai et al.   CLINICAL DYSMORPHOLOGY

Female external genitalia, absent uterus, and probable agonadism in a 46,XY infant with bilateral upper amelia

(2010) Yo-ichiro Ohro et al.   CLINICAL GENETICS

Vascular anastomoses leading to amelia and cutis aplasia in a dizygotic twin pregnancy

(2010) Mary C Phelan et al.   CLINICAL GENETICS

Amelia, cleft lip, and holoprosencephaly: A distinct entity

(2009) Ariana Kariminejad et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Gastrointestinal ramifications of the cloacal exstrophy complex: a 44-year experience

(2009) David Sawaya et al.   JOURNAL OF PEDIATRIC SURGERY

Vertebrate Limb Development: Moving from Classical Morphogen Gradients to an Integrated 4-Dimensional Patterning System

(2009) J.-D. Benazet et al.   Cold Spring Harbor Perspectives in Biology

Genetic Regulation of Embryological Limb Development with Relation to Congenital Limb Deformity in Humans

(2008) Guy Barham et al.   Journal of Childrens Orthopaedics