Y. Izumikawa

发表

16q21 is critical for 16q deletion syndrome

K. Naritomi, N. Shiroma, Y. Izumikawa, 1988, Clinical genetics.

Combined Goltz and Aicardi syndromes in a terminal Xp deletion: are they a contiguous gene syndrome?

Y. Fukushima, N. Niikawa, S. Nagataki, 1992, American journal of medical genetics.

DNA deletion and its parental origin in Angelman syndrome patients.

Y. Fukushima, N. Niikawa, Y. Kuroki, 1991, American journal of medical genetics.

Assignment of the human PAX4 gene to chromosome band 7q32 by fluorescence in situ hybridization.

N. Niikawa, H. Soejima, T. Kishino, 1994, Cytogenetics and cell genetics.

Y‐derived sequence detected in minute chromosomes by polymerase chain reaction and in situ hybridization

F. Kishi, S. Matsuura, T. Kajii, 1992, Clinical Genetics.

Gene assignment of Zellweger syndrome to 7q11.23: report of the second case associated with a pericentric inversion of chromosome 7

N. Shimozawa, Yasuyuki Suzuki, K. Naritomi, 1989, Human Genetics.

Small interstitial deletion of the long arm of chromosome 2 (2q24.3): Further delineation of 2q medial monosomy syndrome

Y. Chinen, K. Naritomi, T. Tohma, 1996, Japanese Journal of Human Genetics.

Trisomy 9q3 syndrome: a case report and review of the literature

K. Naritomi, N. Shiroma, Y. Izumikawa, 1989, Clinical genetics.

Replication asynchrony between homologs 15q11.2: Cytogenetic evidence for genomic imprinting

K. Naritomi, Y. Izumikawa, K. Hirayama, 2005, Human Genetics.

The costello syndrome: A boy with thick mitral valves and arrhythmias

K. Naritomi, T. Tohma, N. Shiroma, 1993, Japanese Journal of Human Genetics.

A comparison of GC content and the proportion of Alu/KpnI-repetitive sequences in a single dark- and light-band region from a human chromosome.

N. Niikawa, K. Yoshiura, H. Soejima, 1994, Genomics.

Diagnostic hand anomalies in Smith-Magenis syndrome: four new patients with del (17)(p11.2p11.2)

N. Niikawa, S. Matsuura, I. Kondo, 1991, American journal of medical genetics.

Apert syndrome with partial polysyndactyly: A proposal on the classification of acrocephalosyndactyly

K. Naritomi, N. Shiroma, Y. Izumikawa, 1988, Japanese Journal of Human Genetics.

Two sisters with Toriello-Carey syndrome.

K. Naritomi, T. Tohma, Y. Izumikawa, 1999, American journal of medical genetics.

Brief Clinical Report Two Sisters With Toriello-Carey Syndrome

Y. Chinen, K. Naritomi, T. Tohma, 1999 .

Sanfilippo type B syndrome: five patients with an R565P homozygous mutation in the α-N-acetylglucosaminidase gene from the Okinawa islands in Japan

Y. Chinen, T. Tohma, Y. Izumikawa, 2005, Journal of Human Genetics.

A Case of 4p Trisomy Syndrome Originated from Maternal rcp(4; | 4)(p | 5. |;p ||.|): An Analysis with CBG, Ag‐NORs and Cd Banding Techniques in Prometaphase Cells

K. Naritomi, Y. Izumikawa, K. Hirayama, 1988 .

Inverted insertion of chromosome 7q and ectrodactyly.

K. Naritomi, T. Tohma, Y. Izumikawa, 1993, American journal of medical genetics.