Human molecular genetics

DLX4 is associated with orofacial clefting and abnormal jaw development.

Human molecular genetics

Wu D, Mandal S, Choi A, Anderson A, Prochazkova M, Perry H, Gil-Da-Silva-Lopes VL, Lao R, Wan E, Tang PL, Kwok PY, Klein O, Zhuan B, Slavotinek AM

Loss of Tbx1 induces bone phenotypes similar to cleidocranial dysplasia.

Human molecular genetics

Funato N, Nakamura M, Richardson JA, Srivastava D, Yanagisawa H

Loss of Tbx1 induces bone phenotypes similar to cleidocranial dysplasia.

Human molecular genetics

Funato N, Nakamura M, Richardson JA, Srivastava D, Yanagisawa H

Functional characterization of SIM1-associated enhancers.

Human molecular genetics

Kim MJ, Oksenberg N, Hoffmann TJ, Vaisse C, Ahituv N

Functional characterization of SIM1-associated enhancers.

Human molecular genetics

Kim MJ, Oksenberg N, Hoffmann TJ, Vaisse C, Ahituv N

Abnormal Ras signaling in Costello syndrome (CS) negatively regulates enamel formation.

Human molecular genetics

Goodwin AF, Tidyman WE, Jheon AH, Sharir A, Zheng X, Charles C, Fagin JA, McMahon M, Diekwisch TG, Ganss B, Rauen KA, Klein OD

Abnormal Ras signaling in Costello syndrome (CS) negatively regulates enamel formation.

Human molecular genetics

Goodwin AF, Tidyman WE, Jheon AH, Sharir A, Zheng X, Charles C, Fagin JA, McMahon M, Diekwisch TG, Ganss B, Rauen KA, Klein OD

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