Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1

Muhammad Farooq; Shahid Baig; Niels Tommerup; Klaus W. Kjaer

doi:10.1002/ajmg.a.33234

Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1

Muhammad Farooq
, Shahid Baig
, Niels Tommerup
, Klaus W. Kjaer

Research output: Contribution to journal › Letter › peer-review

18 Citations (Scopus)

Original language	English (UK)
Pages (from-to)	495-497
Number of pages	3
Journal	American Journal of Medical Genetics, Part A
Volume	152
Issue number	2
DOIs	https://doi.org/10.1002/ajmg.a.33234
Publication status	Published - Feb 2010
Externally published	Yes

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Farooq, M., Baig, S., Tommerup, N., & Kjaer, K. W. (2010). Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1. American Journal of Medical Genetics, Part A, 152(2), 495-497. https://doi.org/10.1002/ajmg.a.33234

Farooq, Muhammad ; Baig, Shahid ; Tommerup, Niels et al. / Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1. In: American Journal of Medical Genetics, Part A. 2010 ; Vol. 152, No. 2. pp. 495-497.

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title = "Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1",

author = "Muhammad Farooq and Shahid Baig and Niels Tommerup and Kjaer, \{Klaus W.\}",

year = "2010",

month = feb,

doi = "10.1002/ajmg.a.33234",

language = "English (UK)",

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Farooq, M, Baig, S, Tommerup, N & Kjaer, KW 2010, 'Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1', American Journal of Medical Genetics, Part A, vol. 152, no. 2, pp. 495-497. https://doi.org/10.1002/ajmg.a.33234

Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1. / Farooq, Muhammad; Baig, Shahid; Tommerup, Niels et al.
In: American Journal of Medical Genetics, Part A, Vol. 152, No. 2, 02.2010, p. 495-497.

Research output: Contribution to journal › Letter › peer-review

TY - JOUR

T1 - Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1

AU - Farooq, Muhammad

AU - Baig, Shahid

AU - Tommerup, Niels

AU - Kjaer, Klaus W.

PY - 2010/2

Y1 - 2010/2

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U2 - 10.1002/ajmg.a.33234

DO - 10.1002/ajmg.a.33234

M3 - Letter

C2 - 20101680

AN - SCOPUS:75449091571

SN - 1552-4825

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SP - 495

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JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

IS - 2

ER -

Farooq M, Baig S, Tommerup N, Kjaer KW. Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1. American Journal of Medical Genetics, Part A. 2010 Feb;152(2):495-497. doi: 10.1002/ajmg.a.33234

Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation and is allelic to premature chromosomal condensation syndrome and primary autosomal recessive microcephaly type 1

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