Frontonasal dysplasia with alar clefts in two sisters. Genetic considerations and surgical correction.

Frontonasal dysplasia with severe occipital lobe hypoplasia.

Radiologic findings of Patterson-Lowry rhizomelic dysplasia in two sisters.

Prenatal diagnosis of frontonasal dysplasia with anterior encephalocele.

Pentalogy of Cantrell, ectopia cordis, and frontonasal dysplasia.

Correction of the pinched nasal tip with alar spreader grafts.

Hydroxyproline metabolism in two sisters with hydroxyprolinemia.

Induction of anesthesia in infant with frontonasal dysplasia and meningoencephalocele: a case report.

Novel homozygous ALX4 mutation causing frontonasal dysplasia-2 in a patient with meningoencephalocele.

Comparison of two models of surgical care for patients with clefts in Peru.

Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome).

Potocki-Shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype.

Lymphoproliferative disease in two sisters.

Heerfordt's syndrome in two sisters.

Multiple myeloma in two sisters.

Prenatal diagnosis of frontonasal dysplasia associated with bilateral periventricular nodular heterotopia.

Tailored Treatment of Colorectal Cancer: Surgical, Molecular, and Genetic Considerations.

Facial clefts and facial dysplasia: revisiting the classification.

A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene.

[Athyreotic congenital hypothyroidism in two sisters].

Pentasomy X mosaic in two adult sisters with diabetes mellitus.

Familial Swyer syndrome in two sisters with undeveloped uterus.

VWD type 2N (Normandy) in two sisters.

Two sisters with generalized dystonia associated with homocystinuria.

Minocycline-induced pigmentation occurring in two sisters.

Suggest Documents

Frontonasal dysplasia with severe occipital lobe hypoplasia.

Radiologic findings of Patterson-Lowry rhizomelic dysplasia in two sisters.

Prenatal diagnosis of frontonasal dysplasia with anterior encephalocele.

Pentalogy of Cantrell, ectopia cordis, and frontonasal dysplasia.

Correction of the pinched nasal tip with alar spreader grafts.

Hydroxyproline metabolism in two sisters with hydroxyprolinemia.

Induction of anesthesia in infant with frontonasal dysplasia and meningoencephalocele: a case report.

Novel homozygous ALX4 mutation causing frontonasal dysplasia-2 in a patient with meningoencephalocele.

Comparison of two models of surgical care for patients with clefts in Peru.

Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome).

Potocki-Shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype.

Lymphoproliferative disease in two sisters.

Heerfordt's syndrome in two sisters.

Multiple myeloma in two sisters.

Prenatal diagnosis of frontonasal dysplasia associated with bilateral periventricular nodular heterotopia.

Tailored Treatment of Colorectal Cancer: Surgical, Molecular, and Genetic Considerations.

Facial clefts and facial dysplasia: revisiting the classification.

A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene.

[Athyreotic congenital hypothyroidism in two sisters].

Pentasomy X mosaic in two adult sisters with diabetes mellitus.

Familial Swyer syndrome in two sisters with undeveloped uterus.

VWD type 2N (Normandy) in two sisters.

Two sisters with generalized dystonia associated with homocystinuria.

Minocycline-induced pigmentation occurring in two sisters.

Frontonasal dysplasia with alar clefts in two sisters. Genetic considerations and surgical correction.

Recommend Documents

Follow Us