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Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromesA novel nonsense mutation of the KAL1 gene (p.Trp204*) in Kallmann syndrome.Erythrocyte membrane antigen frequencies in patients with Type II congenital smell loss.A genetic marker of the ACKR1 gene is present in patients with Type II congenital smell loss who have type I hyposmia and hypogeusia.Renal agenesis in Kallmann syndrome: a network approach.Clinical genetic testing for Kallmann syndrome.Novel homozygous deletion of segmental KAL1 and entire STS cause Kallmann syndrome and X-linked ichthyosis in a Chinese family.
P2860
Q21131272-041B3C4B-67C5-4454-AFE7-3AA50C7208ACQ34337653-6C7454D0-1312-4855-96B7-EF3A3255F942Q35088269-F1081C5A-D088-41ED-9374-2076E0BFF625Q39101877-841D328E-CC0E-4226-A33C-804FBDADDEE5Q39128096-C9B3087D-E0FA-4DDC-807D-64043ECBCB27Q43176450-5071F4F6-B027-4BA9-830B-5942681C0AC1Q45872163-88ADF56F-F0BD-4FFF-9C8C-D7847E5330C0
P2860
description
article científic
@ca
article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on March 2013
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vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
Identification of HESX1 mutations in Kallmann syndrome.
@en
Identification of HESX1 mutations in Kallmann syndrome.
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type
label
Identification of HESX1 mutations in Kallmann syndrome.
@en
Identification of HESX1 mutations in Kallmann syndrome.
@nl
prefLabel
Identification of HESX1 mutations in Kallmann syndrome.
@en
Identification of HESX1 mutations in Kallmann syndrome.
@nl
P2093
P2860
P1476
Identification of HESX1 mutations in Kallmann syndrome.
@en
P2093
Hyung-Goo Kim
Kayce Newbern
Lawrence C Layman
Lisa M Halvorson
Lynn P Chorich
Nithya Natrajan
Richard S Cameron
P2860
P304
P356
10.1016/J.FERTNSTERT.2013.01.149
P407
P577
2013-03-01T00:00:00Z