S E Lloyd - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Filters

S E Lloyd

Showing results (1-10 of 18) with videos related to

Pageof 2

Sort By:

Journal of Experimental Child Psychology|June 1, 1983

Infant search strategies with containers that move but do not alter the location at which contents can be foundS E Lloyd, N H Freeman

The Central African Journal of Medicine|March 1, 1987

Hereditary bleeding disorders in ZimbabweansJ M Mukiibi, S Field, S E Lloyd

Pediatric Nephrology (Berlin, Germany)|August 24, 1999

A familial syndrome due to Arg648Stop mutation in the X-linked renal chloride channel geneM Bosio, M L Bianchi, S E Lloyd, et al.

The Central African Journal of Medicine|May 1, 1996

Haemophilia care in ZimbabweJ O Adewuyi, A M Coutts, L Levy, et al.

Tropical and Geographical Medicine|January 1, 1990

Haemophilia in ZimbabweJ M Mukiibi, B Paul, S P Field, et al.

Human Genetics|May 1, 1997

Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)S E Lloyd, J T Pang, S H Pearce, et al.

American Journal of Human Genetics|January 23, 1999

Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13S E Lloyd, A A Pannett, P H Dixon, et al.

The Journal of Clinical Investigation|March 1, 1997

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)S E Lloyd, S H Pearce, W Günther, et al.

Genomics|October 10, 1995

Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis)S E Fisher, I van Bakel, S E Lloyd, et al.

Human Molecular Genetics|November 1, 1994

Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis)S E Fisher, G C Black, S E Lloyd, et al.

Pageof 2

Search research articles

Showing results (1-10 of 18) with videos related to

Sort By:

Pageof 2

Journal of Experimental Child Psychology|June 1, 1983

Infant search strategies with containers that move but do not alter the location at which contents can be foundS E Lloyd, N H Freeman

The Central African Journal of Medicine|March 1, 1987

Hereditary bleeding disorders in ZimbabweansJ M Mukiibi, S Field, S E Lloyd

Pediatric Nephrology (Berlin, Germany)|August 24, 1999

A familial syndrome due to Arg648Stop mutation in the X-linked renal chloride channel geneM Bosio, M L Bianchi, S E Lloyd, et al.

The Central African Journal of Medicine|May 1, 1996

Haemophilia care in ZimbabweJ O Adewuyi, A M Coutts, L Levy, et al.

Tropical and Geographical Medicine|January 1, 1990

Haemophilia in ZimbabweJ M Mukiibi, B Paul, S P Field, et al.

Human Genetics|May 1, 1997

Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)S E Lloyd, J T Pang, S H Pearce, et al.

American Journal of Human Genetics|January 23, 1999

Localization of familial benign hypercalcemia, Oklahoma variant (FBHOk), to chromosome 19q13S E Lloyd, A A Pannett, P H Dixon, et al.

The Journal of Clinical Investigation|March 1, 1997

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)S E Lloyd, S H Pearce, W Günther, et al.

Genomics|October 10, 1995

Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis)S E Fisher, I van Bakel, S E Lloyd, et al.

Human Molecular Genetics|November 1, 1994

Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis)S E Fisher, G C Black, S E Lloyd, et al.

Pageof 2