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Journal of Human Genetics (21)
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Showing 1–31 of 31 results

Advanced filters: Author: TADASHI KAJII Clear advanced filters

The road to diploid androgenesis

Tadashi Kajii
Research06 Jun 2005
Japanese journal of human genetics

Volume: 31, P: 61-71
Dispermic origin of XY hydatidiform moles

Koso Ohama
Tadashi Kajii
Keiji Hagiwara
Research06 Aug 1981
Nature

Volume: 292, P: 551-552
Physical parameters in Japanese newborns

Hiroshi Tateishi
Tadashi Kajii
Research01 Sept 1992
Japanese Journal of Human Genetics

Volume: 37, P: 223-228
Radiographic measurements of metacarpophalangeal lengths in Japanese children

Shinya Matsuura
Tadashi Kajii
Research01 Jun 1989
Japanese journal of human genetics

Volume: 34, P: 159-168
Normal values for physical parameters of the head, face and hand in Japanese children

Mie Igarashi
Tadashi Kajii
Research01 Mar 1988
Japanese journal of human genetics

Volume: 33, P: 9-31
Silver syndrome: An infant with necropsy findings

Kiyoshi Imaizumi
Tetsuro Ogino
Tadashi Kajii
Research01 Sept 1983
Japanese journal of human genetics

Volume: 28, P: 231-234
Androgenetic origin of hydatidiform mole

TADASHI KAJII
Koso OHAMA
Research18 Aug 1977
Nature

Volume: 268, P: 633-634
Borjeson-Forssman-Lehmann syndrome in a girl

Kiyosato Matsuo
Ichiro Murano
Tadashi Kajii
Research01 Jun 1984
Japanese journal of human genetics

Volume: 29, P: 121-126
Pfeiffer syndrome or Saethre-Chotzen syndrome?

Masato Tsukahara
Keiji Hagiwara
Tadashi Kajii
Research01 Jun 1985
Japanese journal of human genetics

Volume: 30, P: 51-56
Early onset of menstruation in a 45,X girl

Ichiro Murano
Kiyosato Matsuo
Tadashi Kajii
Research14 Jun 2005
Japanese journal of human genetics

Volume: 30, P: 35-40
Technique for Investigation of Sex Chromatin in Amniotic Membrane of Rat Foetuses

ELVIRA FARÍAS
TADASHI KAJII
LYTT I. GARDNER
Research01 Apr 1967
Nature

Volume: 214, P: 499-500
Octocentric Human Ring Chromosome (Xr): Proposed Mechanism of Formation

JOHN F. ELLIS
RICHARD L. NEU
LYTT I. GARDNER
Research07 Sept 1968
Nature

Volume: 219, P: 1071-1072
Neutrophil Adhesion Abnormality with Deficient Surface Membrane Proteins (gp 110 and p 98): The Effect of their Antibodies on the Function of Normal Neutrophils

Kyoko Fujita
Kunihiko Kobayashi
Tadashi Kajii
Research01 Apr 1986
Pediatric Research

Volume: 20, P: 361-366
Autosomal recessive lymphedema?

Tadashi Kajii
Masato Tsukahara
Correspondence01 Mar 1986
Japanese Journal of Human Genetics

Volume: 31, P: 57
Neonatal progeroid syndrome: Report of a Japanese infant

Hirofumi Ohashi
Tsuyako Eguchi
Tadashi Kajii
Research01 Sept 1987
Japanese journal of human genetics

Volume: 32, P: 253-256
Isolation of A Y chromosomal DNA sequence and its clinical application

Masato Tsukahara
Shinya Matsuura
Tadashi Kajii
Research01 Dec 1990
Japanese journal of human genetics

Volume: 35, P: 331-339
Distal arthrogryposis type IIB in a girl: Autosomal recessive inheritance?

Masato Tsukahara
Tadashi Kajii
Research01 Dec 1984
Japanese journal of human genetics

Volume: 29, P: 447-451
Spondylocostal dysostosis: Report of three patients

Hirofumi Ohashi
Yoshitsugu Sugio
Tadashi Kajii
Research01 Dec 1987
Japanese journal of human genetics

Volume: 32, P: 299-303
Common fragile sites induced by folate deprivation, BrdU and aphidicolin: Their frequency and distribution in Japanese individuals

Akira Kuwano
Yoshitsugu Sugio
Tadashi Kajii
Research01 Sept 1988
Japanese journal of human genetics

Volume: 33, P: 355-364
A 7q-son of an XYY father

Tadashi Kajii
Ichiro Murano
Research01 Sept 1984
Japanese Journal of Human Genetics

Volume: 29, P: 387-389
Congenital lymphedema in two siblings

Tadashi Kajii
Masato Tsukahara
Research14 Jun 2005
Japanese journal of human genetics

Volume: 30, P: 31-34
Interstitial pulmonary fibrosis in two sisters. possible autosomal recessive inheritance

Masato Tsukahara
Tadashi Kajii
Research01 Dec 1983
Japanese journal of human genetics

Volume: 28, P: 263-267
Complex chromosome rearrangements: Report of three patients

Tsutomu Kamei
Sei Lee-Okimoto
Norio Niikawa
Research01 Sept 1988
Japanese journal of human genetics

Volume: 33, P: 365-372
Inverted insertion (9)(q34.3q22.3q21.2) and its recombination product: Duplication 9q21.2q22.3

Tadashi Kajii
Shinya Matsuura
Akira Kuwano
Correspondence08 Jun 2005
Japanese journal of human genetics

Volume: 32, P: 45-48
ASSOCIATION OF TRIPHALANGEAL THUMBS, CAFE AU LAIT SPOTS AND LEUKEMIA

Lytt I Gardner
Diane Cass
Tadashi Kajii
Research01 Apr 1977
Pediatric Research

Volume: 11, P: 455
Two Japanese cases with microcephalic primordial dwarfism: Classical seckel syndrome and osteodysplastic primordial dwarfism type II

Yoshitsugu Sugio
Masato Tsukahara
Tadashi Kajii
Research01 Jun 1993
Japanese journal of human genetics

Volume: 38, P: 209-217
Phocomelia With Mandibular Hypoplasia: A New Syndrome

Salma Regina Assemany
Tadashi Kajii
Lytt I Gardner
Research01 Sept 1970
Pediatric Research

Volume: 4, P: 441-442
Molecular analysis of a patient with Beckwith-Wiedemann syndrome, rhabdomyosarcoma and renal cell carcinoma

Tadashi Matsumoto
Ei-ichi Kinoshita
Yoshiro Tsuji
Research01 Jun 1994
Japanese journal of human genetics

Volume: 39, P: 225-234
ANDROGENIC ORIGIN OF HYDATIDIFORM MOLE

Tadashi
Kajii
Lytt I Gardner
Research01 Apr 1977
Pediatric Research

Volume: 11, P: 458
Intranasal oxytocin suppresses seizure-like behaviors in a mouse model of NGLY1 deficiency

Epileptic seizure is one of the symptoms in patients with NGLY1 deficiency, a congenital disorder of deglycosylation. Here the authors show suppressive effects of oxytocin on seizure-like behaviors in a mouse model of NGLY1 deficiency.

Yukimasa Makita
Makoto Asahina
Tadashi Suzuki
ResearchOpen Access22 Apr 2024
Communications Biology

Volume: 7, P: 1-9
Heterozygous TGFBR2 mutations in Marfan syndrome

Takeshi Mizuguchi
Gwenaëlle Collod-Beroud
Naomichi Matsumoto
Research04 Jul 2004
Nature Genetics

Volume: 36, P: 855-860

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