Journal of human genetics

- 日本人類遺伝学会ニホンジンルイイデンガッカイ

Before Rename:1

Author(s)

- 日本人類遺伝学会ニホンジンルイイデンガッカイ

Bibliographic Information

Journal of human genetics

Springer-Verlag Tokyo, c1998-

Vol. 43, no. 1 (1998)-

Other Title: J. Hum. Genet

Access to Electronic Resource 141 items

Journal of human genetics
43(3);1998 1998

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Journal of human genetics
43(1);1998 1998

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Journal of human genetics
43(2);1998 1998

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Journal of human genetics
43(Supplement);1998 1998

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Journal of human genetics
43(4);1998 1998

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Journal of human genetics
44(2);1999 1999

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Journal of human genetics
44(3);1999 1999

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Journal of human genetics
44(5);1999 1999

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Journal of human genetics
44(6);1999 1999

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Journal of human genetics
44(4);1999 1999

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Journal of human genetics
44(1);1999 1999

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Journal of human genetics
45(4);2000 2000

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Journal of human genetics
45(5);2000 2000

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Journal of human genetics
45(1);2000 2000

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Journal of human genetics
45(6);2000 2000

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Journal of human genetics
45(2);2000 2000

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Journal of human genetics
45(3);2000 2000

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Journal of human genetics
46(6);2001 2001

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Journal of human genetics
46(7);2001 2001

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Journal of human genetics
46(3);2001 2001

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Journal of human genetics
46(11);2001 2001

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Journal of human genetics
46(9);2001 2001

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Journal of human genetics
46(1);2001 2001

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Journal of human genetics
46(2);2001 2001

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Journal of human genetics
46(10);2001 2001

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Journal of human genetics
46(8);2001 2001

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Journal of human genetics
46(12);2001 2001

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Journal of human genetics
46(4);2001 2001

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Journal of human genetics
46(5);2001 2001

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Journal of human genetics
47(2);2002 2002

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Journal of human genetics
47(10);2002 2002

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Journal of human genetics
47(3);2002 2002

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Journal of human genetics
47(7);2002 2002

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47(5);2002 2002

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47(6);2002 2002

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47(4);2002 2002

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47(8);2002 2002

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47(1);2002 2002

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48(6);2003 2003

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48(7);2003 2003

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Journal of human genetics
48(11);2003 2003

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Journal of human genetics
48(3);2003 2003

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48(9);2003 2003

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48(8);2003 2003

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Journal of human genetics
48(12);2003 2003

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48(4);2003 2003

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Journal of human genetics
49(2);2004 2004

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Journal of human genetics
49(10);2004 2004

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Journal of human genetics
49(3);2004 2004

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49(11);2004 2004

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49(6);2004 2004

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Journal of human genetics
51(2);2006 2006

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51(10);2006 2006

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51(11);2006 2006

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51(3);2006 2006

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51(7);2006 2006

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51(5);2006 2006

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51(4);2006 2006

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51(8);2006 2006

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51(1);2006 2006

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Journal of human genetics
52(6);2007 2007

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52(7);2007 2007

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52(3);2007 2007

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52(1);2007 2007

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52(4);2007 2007

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52(12);2007 2007

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52(5);2007 2007

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Journal of human genetics
53(10);2008 2008

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Journal of human genetics
53(2);2008 2008

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Journal of human genetics
53(3);2008 2008

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Journal of human genetics
53(11/12);2008 2008

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53(7);2008 2008

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Journal of human genetics
53(5);2008 2008

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Journal of human genetics
53(6);2008 2008

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Journal of human genetics
53(4);2008 2008

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53(8);2008 2008

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Journal of human genetics
53(9);2008 2008

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Journal of human genetics
53(1);2008 2008

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Journal of human genetics
54(7);2009・7 2009

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Journal of human genetics
54(8);2009・8 2009

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Journal of human genetics
54(12);2009・12 2009

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Journal of human genetics
54(4);2009・4 2009

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Journal of human genetics
54(2);2009・2 2009

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Journal of human genetics
54(10);2009・10 2009

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Journal of human genetics
54(3);2009・3 2009

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Journal of human genetics
54(11);2009・11 2009

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Journal of human genetics
54(1);2009・1 2009

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Journal of human genetics
54(9);2009・9 2009

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Journal of human genetics
54(5);2009・5 2009

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Journal of human genetics
54(6);2009・6 2009

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Journal of human genetics
55(11);2010・11 2010

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Journal of human genetics
55(3);2010・3 2010

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Journal of human genetics
55(4);2010・4 2010

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Journal of human genetics
55(12);2010・12 2010

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Journal of human genetics
55(8);2010・8 2010

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Journal of human genetics
55(6);2010・6 2010

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Journal of human genetics
55(7);2010・7 2010

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Journal of human genetics
55(5);2010・5 2010

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Journal of human genetics
55(1);2010・1 2010

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Journal of human genetics
55(9);2010・9 2010

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Journal of human genetics
55(2);2010・2 2010

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Journal of human genetics
55(10)・2010・10 2010

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Precise detection of chromosomal translocation or inversion breakpoints by whole-genome sequencing
2014

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LRRTM4-C538Y novel gene mutation is associated with hereditary macular degeneration with novel dysfunction of ON-type bipolar cells
2018

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Postmortem genetic analysis of sudden unexpected death in infancy:neonatal genetic screening may enable the prevention of sudden infant death
2018.3.31

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Comprehensive genetic analysis of 57 families with clinically suspected Cornelia de Lange syndrome
2019

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Identification of a homozygous frameshift variant in RFLNA in a patient with a typical phenotype of spondylocarpotarsal synostosis syndrome
2020.3.19

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Limited

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Note

Title from cover

Official journal of the Japan Society of Human Genetics

Continues：1

Details

NCID
AA11206160
ISSN
14345161
LCCN
98039238
Country Code
ja
Title Language Code
eng
Text Language Code
eng
Place of Publication
Tokyo
Publication Status
Currently Published Status
Frequency
Quarterly
Regularity
Regular
Type of Continuing Resource
Periodical
Bibliographic History ID
40373000

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