D J Aughton - JoVE Visualize

Showing results (11-20 of 16) with videos related to

Pageof 2

Sort By:

You have reached the last page of results.This site can display upto 16 results.

Clinical Genetics|April 1, 1988

Diploid/tetraploid mosaicism in a liveborn infant demonstrable only in the bone marrow: case report and literature reviewD J Aughton, H M Saal, J A Delach, et al.

The Journal of Pediatrics|February 1, 1995

Transient elevation of sweat chloride concentration in a malnourished girl with the Mauriac syndromeF P Polack, D J Transue, W M Belknap, et al.

American Journal of Medical Genetics|April 15, 1993

Dir dup(X) (q13-->qter) in a girl with growth retardation, microcephaly, developmental delay, seizures, and minor anomaliesD J Aughton, A A AlSaadi, J A Johnson, et al.

Journal of Medical Genetics|December 1, 1990

Nasopharyngeal teratoma ('hairy polyp'), Dandy-Walker malformation, diaphragmatic hernia, and other anomalies in a female infantD J Aughton, C T Sloan, M P Milad, et al.

American Journal of Medical Genetics|January 15, 1994

Prenatal diagnosis of Smith-Lemli-Opitz syndrome, type IIJ A Johnson, D J Aughton, C H Comstock, et al.

Human Molecular Genetics|February 1, 1996

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21U Schell, J Wienberg, A Köhler, et al.

Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 16 results.

Clinical Genetics|April 1, 1988

Diploid/tetraploid mosaicism in a liveborn infant demonstrable only in the bone marrow: case report and literature reviewD J Aughton, H M Saal, J A Delach, et al.

The Journal of Pediatrics|February 1, 1995

Transient elevation of sweat chloride concentration in a malnourished girl with the Mauriac syndromeF P Polack, D J Transue, W M Belknap, et al.

American Journal of Medical Genetics|April 15, 1993

Dir dup(X) (q13-->qter) in a girl with growth retardation, microcephaly, developmental delay, seizures, and minor anomaliesD J Aughton, A A AlSaadi, J A Johnson, et al.

Journal of Medical Genetics|December 1, 1990

Nasopharyngeal teratoma ('hairy polyp'), Dandy-Walker malformation, diaphragmatic hernia, and other anomalies in a female infantD J Aughton, C T Sloan, M P Milad, et al.

American Journal of Medical Genetics|January 15, 1994

Prenatal diagnosis of Smith-Lemli-Opitz syndrome, type IIJ A Johnson, D J Aughton, C H Comstock, et al.

Human Molecular Genetics|February 1, 1996

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21U Schell, J Wienberg, A Köhler, et al.

Pageof 2